A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659121



Internal ID15395773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126759578..127227255hg38UCSC Ensembl
InnerchrX:125893561..126361238hg19UCSC Ensembl
InnerchrX:125721242..126188919hg18UCSC Ensembl
InnerchrX:125619096..126086773hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38467678
hg19467678
hg18467678
hg17467678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519509
Supporting Variants
Samples
Known GenesCXorf64
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659121
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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