Variant Details

Variant: esv2535267

Internal ID

8252139

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr10:73659960..73660154	hg38	UCSC Ensembl
Outer	chr10:73659664..73660518	hg38	UCSC Ensembl
Inner	chr10:75419718..75419912	hg19	UCSC Ensembl
Outer	chr10:75419422..75420276	hg19	UCSC Ensembl
Inner	chr10:75089724..75089918	hg18	UCSC Ensembl
Outer	chr10:75089428..75090282	hg18	UCSC Ensembl

Cytoband

10q22.2

Allele length

Assembly	Allele length
hg38	855
hg19	855
hg18	855

Variant Type

OTHER inversion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5329718

Samples

NA18507

Known Genes

Method

Sequencing

Analysis

Inversions are detected using the AB Inversion Tool. When one end of a mate pair maps to the opposite strand of the other, the pair provides evidence of an inversion. Multiple instances in the same area will be a positive call.

Platform

Not specified

Comments

originalFile=Yoruban_inv.gff

Reference

McKernan_et_al_2009

Pubmed ID

19546169

Accession Number(s)

esv2535267

Frequency

Sample Size	1
Observed Gain	0
Observed Loss	0
Observed Complex	0
Frequency	n/a