A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694889



Internal ID15431541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5205985..5350397hg38UCSC Ensembl
InnerchrX:5124026..5268438hg19UCSC Ensembl
InnerchrX:5134026..5278438hg18UCSC Ensembl
InnerchrX:4983762..5128174hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38144413
hg19144413
hg18144413
hg17144413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522116
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694889
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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