A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515760



Internal ID15442817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:96887520..97148876hg38UCSC Ensembl
InnerchrX:96142519..96403875hg19UCSC Ensembl
InnerchrX:96029175..96290531hg18UCSC Ensembl
InnerchrX:95948664..96210020hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38261357
hg19261357
hg18261357
hg17261357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv520n21
Supporting Variantsnssv690301, nssv663456, nssv694177, nssv664700, nssv691094, nssv703087, nssv662875, nssv690769
Samples
Known GenesDIAPH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515760
Frequency
Sample Size2026
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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