A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615065



Internal ID20988136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112291457..113231778hg38UCSC Ensembl
chr6:112612659..113552980hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38940322
hg19940322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216826
Samples
Known GenesRFPL4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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