A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662875



Internal ID15399527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:96887520..97113312hg38UCSC Ensembl
InnerchrX:96142519..96368311hg19UCSC Ensembl
InnerchrX:96029175..96254967hg18UCSC Ensembl
InnerchrX:95948664..96174456hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38225793
hg19225793
hg18225793
hg17225793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515760
Supporting Variants
Samples
Known GenesDIAPH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662875
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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