A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703087



Internal ID15439739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:97017139..97067488hg38UCSC Ensembl
InnerchrX:96272138..96322487hg19UCSC Ensembl
InnerchrX:96158794..96209143hg18UCSC Ensembl
InnerchrX:96078283..96128632hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3850350
hg1950350
hg1850350
hg1750350
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)nssv703087
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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