A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392733



Internal ID21050286
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 StatusM
Merged Variants
Supporting Variantsnssv18212413
Samples
Known GenesC4orf22, FGF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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