A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213633



Internal ID20780673
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 StatusS
Merged Variantsnsv6383995
Supporting Variants
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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