A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679244



Internal ID15415896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8952896..8987147hg38UCSC Ensembl
InnerchrX:8920937..8955188hg19UCSC Ensembl
InnerchrX:8880937..8915188hg18UCSC Ensembl
InnerchrX:8730673..8764924hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3834252
hg1934252
hg1834252
hg1734252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515590
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679244
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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