A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704156



Internal ID15440808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93276177..93286229hg38UCSC Ensembl
InnerchrX:92531176..92541228hg19UCSC Ensembl
InnerchrX:92417832..92427884hg18UCSC Ensembl
InnerchrX:92337321..92347373hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3810053
hg1910053
hg1810053
hg1710053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516563
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704156
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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