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dbVar

Database of genomic structural variation

nsv5637196

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: 229 SVs from 47 studies. See in: genome view

Submitted genomic100,390,465-100,390,465

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5637196	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	100,390,465	100,390,465
nsv5637196	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	99,726,169	99,726,169

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17133930	insertion	HG00514	Sequencing	Sequence alignment	257

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17133930	Submitted genomic		NC_000005.10:g.100 390465_100390466in s820	GRCh38 (hg38)		NC_000005.10	Chr5	100,390,465	100,390,465
nssv17133930	Remapped	Perfect	NC_000005.9:g.9972 6169_99726170ins82 0	GRCh37.p13	First Pass	NC_000005.9	Chr5	99,726,169	99,726,169

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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