A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383995



Internal ID21041548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41101795..41110514hg38UCSC Ensembl
chr4:41103812..41112531hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg388720
hg198720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213633
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383995
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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