A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939348



Internal ID15886618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36957019..37089312hg38UCSC Ensembl
Innerchr20:35585422..35717715hg19UCSC Ensembl
Innerchr20:35018836..35151129hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38132294
hg19132294
hg18132294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585951
Supporting Variants
Samples
Known GenesRBL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939348
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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