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dbVar

Database of genomic structural variation

nsv5618206

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: 888 SVs from 63 studies. See in: genome view

Submitted genomic1,289,035-1,289,035

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5618206	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	1,289,035	1,289,035
nsv5618206	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	1,224,415	1,224,415

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17060392	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
nssv17060392	Submitted genomic		NC_000001.11:g.128 9035_1289036ins779	GRCh38 (hg38)		NC_000001.11	Chr1	1,289,035	1,289,035
nssv17060392	Remapped	Perfect	NC_000001.10:g.122 4415_1224416ins779	GRCh37.p13	First Pass	NC_000001.10	Chr1	1,224,415	1,224,415

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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