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dbVar

Database of genomic structural variation

esv3662755

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:5,310

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: 986 SVs from 39 studies. See in: genome view

Remapped(Score: Perfect):2,276,982-2,282,291

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3662755	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	2,276,982	2,282,291
esv3662755	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	2,195,023	2,200,332

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16485683	complex substitution	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16485683	Remapped	Perfect	GRCh38.p12	First Pass	NC_000023.11	ChrX	2,276,982	2,282,291
essv16485683	Submitted genomic		GRCh37 (hg19)		NC_000023.10	ChrX	2,195,023	2,200,332

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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