A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212413



Internal ID20779453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80290501..80359200hg38UCSC Ensembl
chr4:81211655..81280354hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3868700
hg1968700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392733
Supporting Variants
Samples
Known GenesC4orf22, FGF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212413
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00076


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