A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526698



Internal ID15453991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87228056..87325691hg38UCSC Ensembl
InnerchrX:86483059..86580694hg19UCSC Ensembl
InnerchrX:86369715..86467350hg18UCSC Ensembl
InnerchrX:86289204..86386839hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3897636
hg1997636
hg1897636
hg1797636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703036
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526698
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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