A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402926



Internal ID21060479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47015619..47021392hg38UCSC Ensembl
chr6:46983355..46989128hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg385774
hg195774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225089
Samples
Known GenesGPR110
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402926
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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