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dbVar

Database of genomic structural variation

nsv6067368

Organism: Homo sapiens

Study:nstd212 (Wu 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):Wu 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: 102 SVs from 28 studies. See in: genome view

Submitted genomic138,091,828-138,091,828

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6067368	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	138,091,828	138,091,828
nsv6067368	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	137,427,517	137,427,517

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17551346	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17551346	Submitted genomic		NC_000005.10:g.138 091828_138091829in s52	GRCh38 (hg38)		NC_000005.10	Chr5	138,091,828	138,091,828
nssv17551346	Remapped	Perfect	NC_000005.9:g.1374 27517_137427518ins 52	GRCh37.p13	First Pass	NC_000005.9	Chr5	137,427,517	137,427,517

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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