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dbVar

Database of genomic structural variation

nsv5655000

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 148 SVs from 27 studies. See in: genome view

Submitted genomic10,293,161-10,293,161

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5655000	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	10,293,161	10,293,161
nsv5655000	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	10,445,760	10,445,760

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17076510	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17076510	Submitted genomic		NC_000012.12:g.102 93161_10293162ins6 1	GRCh38 (hg38)		NC_000012.12	Chr12	10,293,161	10,293,161
nssv17076510	Remapped	Perfect	NC_000012.11:g.104 45760_10445761ins6 1	GRCh37.p13	First Pass	NC_000012.11	Chr12	10,445,760	10,445,760

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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