A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208638



Internal ID20775680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41029..242873hg38UCSC Ensembl
chr3:82701..284556hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38201845
hg19201856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348837
Supporting Variants
Samples
Known GenesCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208638
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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