A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208696



Internal ID20775738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71965276..72037277hg38UCSC Ensembl
chr3:72014427..72086428hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3872002
hg1972002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372818
Supporting Variants
Samples
Known GenesLINC00877
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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