A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526620



Internal ID15107227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:91349713..91604496hg38UCSC Ensembl
InnerchrX:90604712..90859495hg19UCSC Ensembl
InnerchrX:90491368..90746151hg18UCSC Ensembl
InnerchrX:90410857..90665640hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38254784
hg19254784
hg18254784
hg17254784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702940
Samples
Known GenesPABPC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526620
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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