A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696399



Internal ID15086365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:57887251..57916119hg38UCSC Ensembl
InnerchrX:57913685..57942553hg19UCSC Ensembl
InnerchrX:57930410..57959278hg18UCSC Ensembl
InnerchrX:57796706..57825574hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3828869
hg1928869
hg1828869
hg1728869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518933
Supporting Variants
Samples
Known GenesZXDA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696399
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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