A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059615



Internal ID18802146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45719911..45749443hg38UCSC Ensembl
Innerchr20:44348550..44378082hg19UCSC Ensembl
Innerchr20:43781964..43811489hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3829533
hg1929533
hg1829526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n100
Supporting Variantsnssv3584849
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059615
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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