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dbVar

Database of genomic structural variation

nsv5623422

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: 107 SVs from 32 studies. See in: genome view

Submitted genomic65,001,256-65,001,256

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5623422	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	65,001,256	65,001,256
nsv5623422	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	64,986,931	64,986,931

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17126260	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17126260	Submitted genomic		NC_000003.12:g.650 01256_65001257ins3 46	GRCh38 (hg38)		NC_000003.12	Chr3	65,001,256	65,001,256
nssv17126260	Remapped	Perfect	NC_000003.11:g.649 86931_64986932ins3 46	GRCh37.p13	First Pass	NC_000003.11	Chr3	64,986,931	64,986,931

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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