A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212155



Internal ID20779195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183814804..183820977hg38UCSC Ensembl
chr3:183532592..183538765hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg386174
hg196174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363515
Supporting Variants
Samples
Known GenesMAP6D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212155
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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