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dbVar

Database of genomic structural variation

nsv6134120

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:156,069

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: 663 SVs from 66 studies. See in: genome view

Remapped(Score: Perfect):152,331,458-152,487,526

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv6134120	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	152,331,458	152,331,475	152,487,510	152,487,526
nsv6134120	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	153,187,972	153,187,989	153,344,024	153,344,040

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17681295	inversion	SAMN20524660	Sequencing	Paired-end mapping	208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17681295	Remapped	Perfect	NC_000002.12:g.(15 2331458_152331475) _(152487510_152487 526)inv	GRCh38.p12	First Pass	NC_000002.12	Chr2	152,331,458	152,331,475	152,487,510	152,487,526
nssv17681295	Submitted genomic		NC_000002.11:g.(15 3187972_153187989) _(153344024_153344 040)inv	GRCh37 (hg19)		NC_000002.11	Chr2	153,187,972	153,187,989	153,344,024	153,344,040

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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