A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527278



Internal ID15454571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116234513..116297710hg38UCSC Ensembl
InnerchrX:115365768..115428847hg19UCSC Ensembl
InnerchrX:115279796..115342875hg18UCSC Ensembl
InnerchrX:115177650..115240729hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3863198
hg1963080
hg1863080
hg1763080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703688
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527278
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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