A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526098



Internal ID15106705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:13909842..13928837hg38UCSC Ensembl
InnerchrX:13927961..13946956hg19UCSC Ensembl
InnerchrX:13837882..13856877hg18UCSC Ensembl
InnerchrX:13687618..13706613hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3818996
hg1918996
hg1818996
hg1718996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702346
Samples
Known GenesGPM6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526098
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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