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dbVar

Database of genomic structural variation

nsv5629178

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

Submitted genomic44,411,637-44,411,637

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5629178	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	44,411,637	44,411,637
nsv5629178	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	44,379,374	44,379,374

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17155287	insertion	SAMN00007882	Sequencing	Sequence alignment	1,354

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17155287	Submitted genomic		NC_000006.12:g.444 11637_44411638ins5 5	GRCh38 (hg38)		NC_000006.12	Chr6	44,411,637	44,411,637
nssv17155287	Remapped	Perfect	NC_000006.11:g.443 79374_44379375ins5 5	GRCh37.p13	First Pass	NC_000006.11	Chr6	44,379,374	44,379,374

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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