A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520605



Internal ID15447898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:74329492..74349641hg38UCSC Ensembl
InnerchrX:73549327..73569476hg19UCSC Ensembl
InnerchrX:73466052..73486201hg18UCSC Ensembl
InnerchrX:73332348..73352497hg17UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3820150
hg1920150
hg1820150
hg1720150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674965, nssv704597, nssv673041
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520605
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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