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dbVar

Database of genomic structural variation

nsv5648145

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: 314 SVs from 44 studies. See in: genome view

Submitted genomic14,221,302-14,221,302

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5648145	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	14,221,302	14,221,302
nsv5648145	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	14,221,301	14,221,301

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17100310	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17100310	Submitted genomic		NC_000018.10:g.142 21302_14221303ins3 13	GRCh38 (hg38)		NC_000018.10	Chr18	14,221,302	14,221,302
nssv17100310	Remapped	Perfect	NC_000018.9:g.1422 1301_14221302ins31 3	GRCh37.p13	First Pass	NC_000018.9	Chr18	14,221,301	14,221,301

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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