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dbVar

Database of genomic structural variation

nsv5667220

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: 112 SVs from 23 studies. See in: genome view

Submitted genomic30,623,941-30,623,941

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5667220	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	30,623,941	30,623,941
nsv5667220	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	31,019,928	31,019,928

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17136363	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
nssv17136363	Submitted genomic		NC_000022.11:g.306 23941_30623942ins6 9	GRCh38 (hg38)		NC_000022.11	Chr22	30,623,941	30,623,941
nssv17136363	Remapped	Perfect	NC_000022.10:g.310 19928_31019929ins6 9	GRCh37.p13	First Pass	NC_000022.10	Chr22	31,019,928	31,019,928

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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