A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678627



Internal ID15415279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126826893..127239638hg38UCSC Ensembl
InnerchrX:125960876..126373621hg19UCSC Ensembl
InnerchrX:125788557..126201302hg18UCSC Ensembl
InnerchrX:125686411..126099156hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38412746
hg19412746
hg18412746
hg17412746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519509
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678627
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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