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dbVar

Database of genomic structural variation

nsv4436680

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:complex substitution
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:23,405,922

Description:Single allele AND Ductal breast carcinoma

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: 80931 SVs from 143 studies. See in: genome view

Remapped(Score: Good):973,858-24,379,779

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4436680	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	973,858	24,379,779
nsv4436680	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	909,238	24,706,269

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv15754766	complex substitution	Multiple	Multiple	Ductal breast carcinoma	Uncertain significance	ClinVar	RCV000207058.1, VCV000221334.1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15754766	Remapped	Good	GRCh38.p12	First Pass	NC_000001.11	Chr1	973,858	24,379,779
nssv15754766	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	909,238	24,706,269

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv15754766	complex substitution	somatic	Ductal breast carcinoma	Uncertain significance	ClinVar	RCV000207058.1, VCV000221334.1

No genotype data were submitted for this variant

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