A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210117



Internal ID20777157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84662448..84727625hg38UCSC Ensembl
chr3:84711599..84776776hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3865178
hg1965178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375348
Supporting Variants
Samples
Known GenesLINC00971
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210117
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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