A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139147



Internal ID20706187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154245401..154248300hg38UCSC Ensembl
chr6:154566535..154569434hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614711
Supporting Variants
Samples
Known GenesIPCEF1, OPRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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