A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400293



Internal ID21057846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7408178..7409164hg38UCSC Ensembl
chr6:7408411..7409397hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148135
Samples
Known GenesRIOK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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