A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523371



Internal ID15450664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:142018156..142117377hg38UCSC Ensembl
InnerchrX:141105942..141205163hg19UCSC Ensembl
InnerchrX:140933608..141032829hg18UCSC Ensembl
InnerchrX:140831462..140930683hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3899222
hg1999222
hg1899222
hg1799222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699120
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523371
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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