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dbVar

Database of genomic structural variation

nsv5643893

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: 197 SVs from 18 studies. See in: genome view

Submitted genomic132,674,123-132,674,123

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5643893	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	132,674,123	132,674,123
nsv5643893	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	133,686,369	133,686,369

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17153254	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
nssv17153254	Submitted genomic		NC_000008.11:g.132 674123_132674124in s70	GRCh38 (hg38)		NC_000008.11	Chr8	132,674,123	132,674,123
nssv17153254	Remapped	Perfect	NC_000008.10:g.133 686369_133686370in s70	GRCh37.p13	First Pass	NC_000008.10	Chr8	133,686,369	133,686,369

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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