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dbVar

Database of genomic structural variation

esv1533992

Organism: Homo sapiens

Study:estd22 (Levy et al. 2007)
Variant Type:inversion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:9,625

Publication(s):Levy et al. 2007

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: 111 SVs from 31 studies. See in: genome view

Remapped(Score: Good):50,887,960-50,897,584

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv1533992	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	50,887,960	50,897,584
esv1533992	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	50,925,351	50,934,975
esv1533992	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000003.10	Chr3	50,900,409	50,910,036

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv3727871	inversion	HuRef	Sequencing	Sequence alignment	780,358

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv3727871	Remapped	Good	NC_000003.12:g.508 87960_50897584inv	GRCh38.p12	First Pass	NC_000003.12	Chr3	50,887,960	50,897,584
essv3727871	Remapped	Good	NC_000003.11:g.509 25351_50934975inv	GRCh37.p13	First Pass	NC_000003.11	Chr3	50,925,351	50,934,975
essv3727871	Submitted genomic		NC_000003.10:g.509 00409_50910036inv	NCBI36 (hg18)		NC_000003.10	Chr3	50,900,409	50,910,036

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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