A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208629



Internal ID20775671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164764001..164803800hg38UCSC Ensembl
chr3:164481789..164521588hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839800
hg1939800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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