A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524833



Internal ID15452126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45168228..45174875hg38UCSC Ensembl
InnerchrX:45027473..45034120hg19UCSC Ensembl
InnerchrX:44912417..44919064hg18UCSC Ensembl
InnerchrX:44783727..44790374hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg386648
hg196648
hg186648
hg176648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700834
Samples
Known GenesCXorf36
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524833
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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