A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586645



Internal ID16374054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63741460..63778360hg38UCSC Ensembl
Innerchr20:62372813..62409713hg19UCSC Ensembl
Innerchr20:61843257..61880157hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3836901
hg1936901
hg1836901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7684n54
Supporting Variantsnssv1150974
SamplesHGDP00655
Known GenesSLC2A4RG, ZBTB46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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