A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697891



Internal ID15087857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141353297..141388477hg38UCSC Ensembl
InnerchrX:140447446..140482636hg19UCSC Ensembl
InnerchrX:140275112..140310302hg18UCSC Ensembl
InnerchrX:140172966..140208156hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3835181
hg1935191
hg1835191
hg1735191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697891
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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