A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208242



Internal ID20775282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19660913..20013456hg38UCSC Ensembl
chr2:19860674..20213217hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38352544
hg19352544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339202
Supporting Variants
Samples
Known GenesLINC00954, MATN3, TTC32, WDR35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208242
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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