Variant Details

Variant: esv2571440

Internal ID

8634998

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:95149228..95149527	hg38	UCSC Ensembl
Outer	chr15:95147781..95149599	hg38	UCSC Ensembl
Inner	chr15:95692457..95692756	hg19	UCSC Ensembl
Outer	chr15:95691010..95692828	hg19	UCSC Ensembl
Inner	chr15:93493461..93493760	hg18	UCSC Ensembl
Outer	chr15:93492014..93493832	hg18	UCSC Ensembl

Cytoband

15q26.2

Allele length

Assembly	Allele length
hg38	1819
hg19	1819
hg18	1819

Variant Type

OTHER inversion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5316242

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)

esv2571440

Frequency

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