A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521252



Internal ID15448545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87797310..87867862hg38UCSC Ensembl
InnerchrX:87052310..87122862hg19UCSC Ensembl
InnerchrX:86938966..87009518hg18UCSC Ensembl
InnerchrX:86858455..86929007hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3870553
hg1970553
hg1870553
hg1770553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697869
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521252
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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