A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689476



Internal ID15426128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121616028..121787823hg38UCSC Ensembl
InnerchrX:120749882..120921676hg19UCSC Ensembl
InnerchrX:120577563..120749357hg18UCSC Ensembl
InnerchrX:120475417..120647211hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38171796
hg19171795
hg18171795
hg17171795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520535
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689476
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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