A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378862



Internal ID21036415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54740280..54771563hg38UCSC Ensembl
chr4:55606446..55637729hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3831284
hg1931284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211936
Samples
Known GenesKIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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