A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687736



Internal ID15077702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131294015..131346274hg38UCSC Ensembl
InnerchrX:130427989..130480248hg19UCSC Ensembl
InnerchrX:130255670..130307929hg18UCSC Ensembl
InnerchrX:130153524..130205783hg17UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3852260
hg1952260
hg1852260
hg1752260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520550
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687736
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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