A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528528



Internal ID15455821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:4957436..5016758hg38UCSC Ensembl
InnerchrX:4875477..4934799hg19UCSC Ensembl
InnerchrX:4885477..4944799hg18UCSC Ensembl
InnerchrX:4735213..4794535hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3859323
hg1959323
hg1859323
hg1759323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705139
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528528
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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