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dbVar

Database of genomic structural variation

nsv5032617

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:mobile element deletion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:6,530

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: 209 SVs from 57 studies. See in: genome view

Submitted genomic127,094,649-127,101,307

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5032617	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	127,094,728 (-79, +129)	127,101,257 (-72, +50)
nsv5032617	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	127,579,273 (-79, +129)	127,585,802 (-72, +50)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16541288	line1 deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16541288	Submitted genomic		NC_000012.12:g.(12 7094649_127094857) _(127101185_127101 307)del	GRCh38 (hg38)		NC_000012.12	Chr12	127,094,728 (-79, +129)	127,101,257 (-72, +50)
nssv16541288	Remapped	Perfect	NC_000012.11:g.(12 7579194_127579402) _(127585730_127585 852)del	GRCh37.p13	First Pass	NC_000012.11	Chr12	127,579,273 (-79, +129)	127,585,802 (-72, +50)

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)
nssv16541288	0.004	112	29246

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