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dbVar

Database of genomic structural variation

nsv5618601

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: 174 SVs from 25 studies. See in: genome view

Submitted genomic179,783,732-179,783,732

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5618601	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	179,783,732	179,783,732
nsv5618601	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	179,752,867	179,752,867

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17061420	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
nssv17061420	Submitted genomic		NC_000001.11:g.179 783732_179783733in s100	GRCh38 (hg38)		NC_000001.11	Chr1	179,783,732	179,783,732
nssv17061420	Remapped	Perfect	NC_000001.10:g.179 752867_179752868in s100	GRCh37.p13	First Pass	NC_000001.10	Chr1	179,752,867	179,752,867

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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