A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055212



Internal ID18797743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37394136..37466486hg38UCSC Ensembl
Innerchr20:36022539..36094888hg19UCSC Ensembl
Innerchr20:35455953..35528302hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3872351
hg1972350
hg1872350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4306n100
Supporting Variantsnssv3584764
Samples
Known GenesSRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055212
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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