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dbVar

Database of genomic structural variation

nsv4416506

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:659,760

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: 2761 SVs from 105 studies. See in: genome view

Remapped(Score: Perfect):22,757,080-23,416,839

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv4416506	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	22,757,080	22,765,028	23,285,897	23,416,839
nsv4416506	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	23,331,219	23,339,167	23,860,036	23,990,978

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15709144	copy number gain	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15709144	Remapped	Perfect	NC_000013.11:g.(22 757080_22765028)_( 23285897_23416839) dup	GRCh38.p12	First Pass	NC_000013.11	Chr13	22,757,080	22,765,028	23,285,897	23,416,839
nssv15709144	Submitted genomic		NC_000013.10:g.(23 331219_23339167)_( 23860036_23990978) dup	GRCh37 (hg19)		NC_000013.10	Chr13	23,331,219	23,339,167	23,860,036	23,990,978

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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