A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212176



Internal ID20779216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185062710..185114981hg38UCSC Ensembl
chr3:184780498..184832769hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3852272
hg1952272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356512
Supporting Variants
Samples
Known GenesC3orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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