A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520379



Internal ID15447672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33916635..34020958hg38UCSC Ensembl
InnerchrX:33934752..34039075hg19UCSC Ensembl
InnerchrX:33844673..33948996hg18UCSC Ensembl
InnerchrX:33694409..33798732hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38104324
hg19104324
hg18104324
hg17104324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696466, nssv676708, nssv663390
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520379
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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