A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697855



Internal ID15434507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112237770..112261087hg38UCSC Ensembl
InnerchrX:111480998..111504315hg19UCSC Ensembl
InnerchrX:111367654..111390971hg18UCSC Ensembl
InnerchrX:111287143..111310460hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3823318
hg1923318
hg1823318
hg1723318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516845
Supporting Variants
Samples
Known GenesZCCHC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697855
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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