A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212943



Internal ID20779983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63053601..63211700hg38UCSC Ensembl
chr3:63039277..63197376hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38158100
hg19158100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373686
Supporting Variants
Samples
Known GenesLINC00698
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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