A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214753



Internal ID20781793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86845822..86949507hg38UCSC Ensembl
chr4:87766975..87870659hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38103686
hg19103685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379943
Supporting Variants
Samples
Known GenesAFF1, C4orf36, LOC100506746, SLC10A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214753
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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