A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140182



Internal ID20707222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142833363..142833559hg38UCSC Ensembl
chr6:143154500..143154696hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609315
Supporting Variants
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00158


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