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dbVar

Database of genomic structural variation

esv3666931

Organism: Homo sapiens

Study:estd217 (Besenbacher et al. 2015)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:297

Publication(s):Besenbacher et al. 2015

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: 159 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):13,062,977-13,063,273

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3666931	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	13,062,977	13,063,273
esv3666931	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	13,104,977	13,105,273

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16489441	inversion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16489441	Remapped	Perfect	NC_000010.11:g.130 62977_13063273inv2 96	GRCh38.p12	First Pass	NC_000010.11	Chr10	13,062,977	13,063,273
essv16489441	Submitted genomic		NC_000010.10:g.131 04977_13105273inv2 96	GRCh37 (hg19)		NC_000010.10	Chr10	13,104,977	13,105,273

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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