A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694301



Internal ID15430953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:86918470..86957790hg38UCSC Ensembl
InnerchrX:86173473..86212793hg19UCSC Ensembl
InnerchrX:86060129..86099449hg18UCSC Ensembl
InnerchrX:85979618..86018938hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg3839321
hg1939321
hg1839321
hg1739321
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519045
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694301
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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