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dbVar

Database of genomic structural variation

nsv5644609

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: 136 SVs from 28 studies. See in: genome view

Submitted genomic35,836,053-35,836,053

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5644609	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	35,836,053	35,836,053
nsv5644609	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	36,326,955	36,326,955

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17104618	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17104618	Submitted genomic		NC_000019.10:g.358 36053_35836054ins4 47	GRCh38 (hg38)		NC_000019.10	Chr19	35,836,053	35,836,053
nssv17104618	Remapped	Perfect	NC_000019.9:g.3632 6955_36326956ins44 7	GRCh37.p13	First Pass	NC_000019.9	Chr19	36,326,955	36,326,955

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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