A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673860



Internal ID15063826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:106983213..107225478hg38UCSC Ensembl
InnerchrX:106226443..106468708hg19UCSC Ensembl
InnerchrX:106113099..106355364hg18UCSC Ensembl
InnerchrX:106032588..106274853hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38242266
hg19242266
hg18242266
hg17242266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519484
Supporting Variants
Samples
Known GenesMORC4, NUP62CL, PIH1D3, RBM41
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673860
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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