A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523487



Internal ID15450780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140572317..140621607hg38UCSC Ensembl
InnerchrX:139654482..139703772hg19UCSC Ensembl
InnerchrX:139482148..139531438hg18UCSC Ensembl
InnerchrX:139380002..139429292hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3849291
hg1949291
hg1849291
hg1749291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699254
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523487
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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