A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522092



Internal ID15102699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23431718..23515102hg38UCSC Ensembl
InnerchrX:23449835..23533219hg19UCSC Ensembl
InnerchrX:23359756..23443140hg18UCSC Ensembl
InnerchrX:23209492..23292876hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3883385
hg1983385
hg1883385
hg1783385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694864
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522092
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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