A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521056



Internal ID15101663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28590019..28664578hg38UCSC Ensembl
InnerchrX:28608136..28682695hg19UCSC Ensembl
InnerchrX:28518057..28592616hg18UCSC Ensembl
InnerchrX:28367793..28442352hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3874560
hg1974560
hg1874560
hg1774560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697759
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521056
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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