A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518551



Internal ID15099158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7857284..8383635hg38UCSC Ensembl
InnerchrX:7825325..8351676hg19UCSC Ensembl
InnerchrX:7785325..8311676hg18UCSC Ensembl
InnerchrX:7635061..8161412hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38526352
hg19526352
hg18526352
hg17526352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv499n21
Supporting Variantsnssv695994
Samples
Known GenesMIR651, PNPLA4, VCX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518551
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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