A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065548



Internal ID19154767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15991152..16042441hg38UCSC Ensembl
Innerchr20:15971797..16023086hg19UCSC Ensembl
Innerchr20:15919797..15971086hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3851290
hg1951290
hg1851290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599638
Samples
Known GenesMACROD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065548
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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