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dbVar

Database of genomic structural variation

nsv5026689

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:7,301

Publication(s):Abel et al. 2020

Links to Other Resources

Overlapping Genes

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: 304 SVs from 28 studies. See in: genome view

Submitted genomic12,709,234-12,716,593

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5026689	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	12,709,264 (-30, +56)	12,716,564 (-79, +29)
nsv5026689	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	12,709,263 (-30, +56)	12,716,563 (-79, +29)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16569239	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16569239	Submitted genomic		NC_000018.10:g.(12 709234_12709320)_( 12716485_12716593) del	GRCh38 (hg38)		NC_000018.10	Chr18	12,709,264 (-30, +56)	12,716,564 (-79, +29)
nssv16569239	Remapped	Perfect	NC_000018.9:g.(127 09233_12709319)_(1 2716484_12716592)d el	GRCh37.p13	First Pass	NC_000018.9	Chr18	12,709,263 (-30, +56)	12,716,563 (-79, +29)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16569239	<0.001	2	29246

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