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dbVar

Database of genomic structural variation

nsv4681044

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:21,115

Description:NC_000002.12:g.(?_108719587)_(108740701_?)del AND Familial acute necrotizing encephalopathy

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 211 SVs from 38 studies. See in: genome view

Remapped(Score: Perfect):108,719,587-108,740,701

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4681044	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	108,719,587	108,740,701
nsv4681044	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	109,336,043	109,357,157

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv16212427	deletion	Multiple	Multiple	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3; Encephalopathy, acute, infection-induced, 3, suceptibility to; Familial acute necrotizing encephalopathy	Uncertain significance	ClinVar	RCV001033268.2, VCV000832796.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16212427	Remapped	Perfect	NC_000002.12:g.(?_ 108719587)_(108740 701_?)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	108,719,587	108,740,701
nssv16212427	Submitted genomic		NC_000002.11:g.(?_ 109336043)_(109357 157_?)del	GRCh37 (hg19)		NC_000002.11	Chr2	109,336,043	109,357,157

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	HGVS	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv16212427	GRCh37: NC_000002.11:g.(?_109336043)_(109357157_?)del	deletion	germline	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3; Encephalopathy, acute, infection-induced, 3, suceptibility to; Familial acute necrotizing encephalopathy	Uncertain significance	ClinVar	RCV001033268.2, VCV000832796.2

No genotype data were submitted for this variant

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