A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211976



Internal ID20779016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119233849..119330597hg38UCSC Ensembl
chr4:120155004..120251752hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3896749
hg1996749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383699
Supporting Variants
Samples
Known GenesC4orf3, FABP2, USP53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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