A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585347



Internal ID16372756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6045834..6046780hg38UCSC Ensembl
Innerchr20:6026480..6027426hg19UCSC Ensembl
Innerchr20:5974480..5975426hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38947
hg19947
hg18947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7451n54
Supporting Variantsnssv937565, nssv937562, nssv937563, nssv937564, nssv937561
Samples
Known GenesLRRN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585347
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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