A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148933



Internal ID20715973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77807363..77808048hg38UCSC Ensembl
chr6:78517080..78517765hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398836
Supporting Variants
Samples
Known GenesMEI4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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