A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118399



Internal ID20685439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5602756..5610458hg38UCSC Ensembl
chr4:5604483..5612185hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg387703
hg197703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374000
Supporting Variants
Samples
Known GenesEVC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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