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dbVar

Database of genomic structural variation

nsv5671225

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:inversion
Method Type:Optical mapping, Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:121,097

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: 430 SVs from 54 studies. See in: genome view

Submitted genomic124,425,561-124,546,657

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671225	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	124,425,561	124,546,657
nsv5671225	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	123,761,254	123,882,350

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17124835	inversion	HG02818	Optical mapping, Sequencing	Optical mapping, Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17124835	Submitted genomic		NC_000005.10:g.124 425561_124546657in v	GRCh38 (hg38)		NC_000005.10	Chr5	124,425,561	124,546,657
nssv17124835	Remapped	Perfect	NC_000005.9:g.1237 61254_123882350inv	GRCh37.p13	First Pass	NC_000005.9	Chr5	123,761,254	123,882,350

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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