A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064751



Internal ID18807282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59129324..59163840hg38UCSC Ensembl
Innerchr20:57704379..57738895hg19UCSC Ensembl
Innerchr20:57137774..57172290hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3834517
hg1934517
hg1834517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584248
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064751
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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