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dbVar

Database of genomic structural variation

nsv6108772

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: 109 SVs from 15 studies. See in: genome view

Submitted genomic34,442,441-34,442,441

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6108772	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	34,442,441	34,442,441
nsv6108772	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	34,933,346	34,933,346

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17635792	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17635792	Submitted genomic		NC_000019.10:g.344 42441_34442442ins2 85	GRCh38 (hg38)		NC_000019.10	Chr19	34,442,441	34,442,441
nssv17635792	Remapped	Perfect	NC_000019.9:g.3493 3346_34933347ins28 5	GRCh37.p13	First Pass	NC_000019.9	Chr19	34,933,346	34,933,346

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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