A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700834



Internal ID15437486
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 StatusS
Merged Variantsnsv524833
Supporting Variants
Samples
Known GenesCXorf36
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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