A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527249



Internal ID15454542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140804926..140856435hg38UCSC Ensembl
InnerchrX:139887091..139938600hg19UCSC Ensembl
InnerchrX:139714757..139766266hg18UCSC Ensembl
InnerchrX:139612611..139664120hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3851510
hg1951510
hg1851510
hg1751510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703651
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527249
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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