A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464627



Internal ID21122180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77652592..77688163hg38UCSC Ensembl
chr11:77363637..77399208hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3835572
hg1935572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178379
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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