A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676366



Internal ID15066332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43170260..43499806hg38UCSC Ensembl
InnerchrX:43029509..43359055hg19UCSC Ensembl
InnerchrX:42914453..43243999hg18UCSC Ensembl
InnerchrX:42785763..43115309hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38329547
hg19329547
hg18329547
hg17329547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517077
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676366
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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