A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678039



Internal ID15068005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43170260..43458141hg38UCSC Ensembl
InnerchrX:43029509..43317390hg19UCSC Ensembl
InnerchrX:42914453..43202334hg18UCSC Ensembl
InnerchrX:42785763..43073644hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38287882
hg19287882
hg18287882
hg17287882
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)nssv678039
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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