A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520655



Internal ID15101262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30321210..30441396hg38UCSC Ensembl
InnerchrX:30339327..30459513hg19UCSC Ensembl
InnerchrX:30249248..30369434hg18UCSC Ensembl
InnerchrX:30098984..30219170hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38120187
hg19120187
hg18120187
hg17120187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv505n21
Supporting Variantsnssv673595, nssv696104, nssv687571
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520655
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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