A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139790



Internal ID20706830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155512401..155520400hg38UCSC Ensembl
chr6:155833535..155841534hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00094


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