A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585344



Internal ID16372753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6045729..6046674hg38UCSC Ensembl
Innerchr20:6026375..6027320hg19UCSC Ensembl
Innerchr20:5974375..5975320hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38946
hg19946
hg18946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7451n54
Supporting Variantsnssv937558
Samples
Known GenesLRRN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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