A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057376



Internal ID19146595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16587417..16605422hg38UCSC Ensembl
Innerchr20:16568062..16586067hg19UCSC Ensembl
Innerchr20:16516062..16534067hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3818006
hg1918006
hg1818006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4281n100
Supporting Variantsnssv3599645
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)nsv1057376
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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