A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379673



Internal ID21037226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174295078..174332994hg38UCSC Ensembl
chr4:175216229..175254145hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3837917
hg1937917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214652
Samples
Known GenesCEP44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379673
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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