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dbVar

Database of genomic structural variation

nsv4424086

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:2,252

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: 277 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):78,601,267-78,603,518

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
nsv4424086	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	78,601,267	78,601,611	78,603,518	78,603,518
nsv4424086	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	79,175,402	79,175,746	79,177,653	79,177,653

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15720815	copy number loss	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
nssv15720815	Remapped	Perfect	NC_000013.11:g.(78 601267_78601611)_( 78603518_78603518) del	GRCh38.p12	First Pass	NC_000013.11	Chr13	78,601,267	78,601,611	78,603,518	78,603,518
nssv15720815	Submitted genomic		NC_000013.10:g.(79 175402_79175746)_( 79177653_79177653) del	GRCh37 (hg19)		NC_000013.10	Chr13	79,175,402	79,175,746	79,177,653	79,177,653

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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