A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527546



Internal ID15454839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116277031..116393087hg38UCSC Ensembl
InnerchrX:115408287..115524235hg19UCSC Ensembl
InnerchrX:115322315..115438263hg18UCSC Ensembl
InnerchrX:115220169..115336117hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38116057
hg19115949
hg18115949
hg17115949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704007
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527546
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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