A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585945



Internal ID16026668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36894776..36895751hg38UCSC Ensembl
Innerchr20:35523179..35524154hg19UCSC Ensembl
Innerchr20:34956593..34957568hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38976
hg19976
hg18976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7563n54
Supporting Variantsnssv939332
Samples
Known GenesSAMHD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585945
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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