A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212906



Internal ID20779946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:334778..431155hg38UCSC Ensembl
chr4:328567..424944hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3896378
hg1996378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369173
Supporting Variants
Samples
Known GenesABCA11P, ZNF141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212906
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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