A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688460



Internal ID15425112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:20739774..21013311hg38UCSC Ensembl
InnerchrX:20757892..21031429hg19UCSC Ensembl
InnerchrX:20667813..20941350hg18UCSC Ensembl
InnerchrX:20517549..20791086hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38273538
hg19273538
hg18273538
hg17273538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517746
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688460
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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