A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383521



Internal ID21041074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86883760..86906772hg38UCSC Ensembl
chr4:87804913..87827925hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3823013
hg1923013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121749
Samples
Known GenesC4orf36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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