A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696460



Internal ID15433112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33865586..34011813hg38UCSC Ensembl
InnerchrX:33883703..34029930hg19UCSC Ensembl
InnerchrX:33793624..33939851hg18UCSC Ensembl
InnerchrX:33643360..33789587hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38146228
hg19146228
hg18146228
hg17146228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518993
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696460
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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