A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697611



Internal ID15434263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112261087..112348778hg38UCSC Ensembl
InnerchrX:111504315..111592006hg19UCSC Ensembl
InnerchrX:111390971..111478662hg18UCSC Ensembl
InnerchrX:111310460..111398151hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3887692
hg1987692
hg1887692
hg1787692
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)nssv697611
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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