A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211617



Internal ID20778657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6643161..6645271hg38UCSC Ensembl
chr4:6644888..6646998hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg382111
hg192111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374332
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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