A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207680



Internal ID20774720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77949956..78018485hg38UCSC Ensembl
chr2:78177082..78245611hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3868530
hg1968530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346328
Supporting Variants
Samples
Known GenesSNAR-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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