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dbVar

Database of genomic structural variation

nsv5625171

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: 458 SVs from 49 studies. See in: genome view

Submitted genomic137,436,339-137,436,339

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5625171	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	137,436,339	137,436,339
nsv5625171	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	140,330,791	140,330,791

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17160947	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
nssv17160947	Submitted genomic		NC_000009.12:g.137 436339_137436340in s53	GRCh38 (hg38)		NC_000009.12	Chr9	137,436,339	137,436,339
nssv17160947	Remapped	Perfect	NC_000009.11:g.140 330791_140330792in s53	GRCh37.p13	First Pass	NC_000009.11	Chr9	140,330,791	140,330,791

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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