A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528629



Internal ID15455922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145203465..145241117hg38UCSC Ensembl
InnerchrX:144284985..144322637hg19UCSC Ensembl
InnerchrX:144092677..144130329hg18UCSC Ensembl
InnerchrX:143990531..144028183hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3837653
hg1937653
hg1837653
hg1737653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705259
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528629
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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