A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661646



Internal ID15398298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23033043..23078450hg38UCSC Ensembl
InnerchrX:23051160..23096567hg19UCSC Ensembl
InnerchrX:22961081..23006488hg18UCSC Ensembl
InnerchrX:22810817..22856224hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3845408
hg1945408
hg1845408
hg1745408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520197
Supporting Variants
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661646
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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