A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212128



Internal ID20779168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15479530..15484047hg38UCSC Ensembl
chr4:15481154..15485671hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362858
Supporting Variants
Samples
Known GenesCC2D2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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