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dbVar

Database of genomic structural variation

nsv6637824

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:119,836

Description:GRCh37/hg19 21q22.12(chr21:36045253-36165086)x3 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: 398 SVs from 52 studies. See in: genome view

Remapped(Score: Good):34,672,954-34,792,789

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6637824	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	34,672,954	34,792,789
nsv6637824	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	36,045,253	36,165,086

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv18329934	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV002473666.1, VCV001808349.1	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18329934	Remapped	Good	NC_000021.9:g.(?_3 4672954)_(34792789 _?)dup	GRCh38.p12	First Pass	NC_000021.9	Chr21	34,672,954	34,792,789
nssv18329934	Submitted genomic		NC_000021.8:g.(?_3 6045253)_(36165086 _?)dup	GRCh37 (hg19)		NC_000021.8	Chr21	36,045,253	36,165,086

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
nssv18329934	GRCh37: NC_000021.8:g.(?_36045253)_(36165086_?)dup	copy number gain	unknown	not provided	Uncertain significance	ClinVar	RCV002473666.1, VCV001808349.1	3

No genotype data were submitted for this variant

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