A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166567



Internal ID20733607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139638572..139640914hg38UCSC Ensembl
chr8:140650815..140653157hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382343
hg192343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416727
Supporting Variants
Samples
Known GenesKCNK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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