A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065355



Internal ID19154574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23744891..23816014hg38UCSC Ensembl
Innerchr20:23725528..23796651hg19UCSC Ensembl
Innerchr20:23673528..23744651hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3871124
hg1971124
hg1871124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4287n100
Supporting Variantsnssv3584670, nssv3584669, nssv3584671
Samples
Known GenesCST1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065355
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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