A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117046



Internal ID20684086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39761274..39763340hg38UCSC Ensembl
chr4:39762894..39764960hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382067
hg192067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378408
Supporting Variants
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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