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dbVar

Database of genomic structural variation

nsv3873905

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:524,097

Description:GRCh37/hg19 3q11.2(chr3:97650137-98174233)x3 AND See cases

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: 1556 SVs from 86 studies. See in: genome view

Remapped(Score: Perfect):97,931,293-98,455,389

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3873905	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	97,931,293	98,455,389
nsv3873905	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	97,650,137	98,174,233

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15151869	copy number gain	Multiple	Multiple	See cases	Uncertain significance	ClinVar	RCV000512476.2, VCV000443897.2	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15151869	Remapped	Perfect	NC_000003.12:g.(?_ 97931293)_(9845538 9_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	97,931,293	98,455,389
nssv15151869	Submitted genomic		NC_000003.11:g.(?_ 97650137)_(9817423 3_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	97,650,137	98,174,233

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
nssv15151869	GRCh37: NC_000003.11:g.(?_97650137)_(98174233_?)dup	copy number gain	not provided	See cases	Uncertain significance	ClinVar	RCV000512476.2, VCV000443897.2	3

No genotype data were submitted for this variant

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