Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4456795

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:129,670

Description:GRCh37/hg19 7q21.11(chr7:80427529-80557198)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: 353 SVs from 54 studies. See in: genome view

Remapped(Score: Perfect):80,798,213-80,927,882

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4456795	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	80,798,213	80,927,882
nsv4456795	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	80,427,529	80,557,198

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15773615	copy number loss	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV000849966.2, VCV000689275.2	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15773615	Remapped	Perfect	NC_000007.14:g.(?_ 80798213)_(8092788 2_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	80,798,213	80,927,882
nssv15773615	Submitted genomic		NC_000007.13:g.(?_ 80427529)_(8055719 8_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	80,427,529	80,557,198

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
nssv15773615	GRCh37: NC_000007.13:g.(?_80427529)_(80557198_?)del	copy number loss	unknown	not provided	Uncertain significance	ClinVar	RCV000849966.2, VCV000689275.2	1

No genotype data were submitted for this variant

You are here: NCBI