A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062713



Internal ID19151932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53546616..53564213hg38UCSC Ensembl
Innerchr20:52163155..52180752hg19UCSC Ensembl
Innerchr20:51596562..51614159hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3817598
hg1917598
hg1817598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586081
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)nsv1062713
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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