A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209772



Internal ID20776813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42834022..42839417hg38UCSC Ensembl
chr2:43061162..43066557hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg385396
hg195396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6338187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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