A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062914



Internal ID19152133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4053692..4096572hg38UCSC Ensembl
Innerchr20:4034339..4077219hg19UCSC Ensembl
Innerchr20:3982339..4025219hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3842881
hg1942881
hg1842881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599350
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)nsv1062914
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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