A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116064



Internal ID20683104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39067070..39073952hg38UCSC Ensembl
chr4:39068690..39075572hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386883
hg196883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382263
Supporting Variants
Samples
Known GenesKLHL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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