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dbVar

Database of genomic structural variation

nsv3886606

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:68,978

Description:GRCh37/hg19 1p21.3(chr1:99164334-99233311)x1 AND not provided

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: 266 SVs from 52 studies. See in: genome view

Remapped(Score: Perfect):98,698,778-98,767,755

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3886606	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	98,698,778	98,767,755
nsv3886606	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	99,164,334	99,233,311

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15153291	copy number loss	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV000684607.1, VCV000565132.1	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15153291	Remapped	Perfect	NC_000001.11:g.(?_ 98698778)_(9876775 5_?)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	98,698,778	98,767,755
nssv15153291	Submitted genomic		NC_000001.10:g.(?_ 99164334)_(9923331 1_?)del	GRCh37 (hg19)		NC_000001.10	Chr1	99,164,334	99,233,311

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	Copy number
nssv15153291	GRCh37: NC_000001.10:g.(?_99164334)_(99233311_?)del	copy number loss	germline	not provided	Uncertain significance	ClinVar	RCV000684607.1, VCV000565132.1	1

No genotype data were submitted for this variant

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