A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585958



Internal ID16373367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37376872..37435163hg38UCSC Ensembl
Innerchr20:36005275..36063565hg19UCSC Ensembl
Innerchr20:35438689..35496979hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3858292
hg1958291
hg1858291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7566n54
Supporting Variantsnssv1151353
SamplesNINDS_136
Known GenesSRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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