A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206372



Internal ID20773412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61623110..61636560hg38UCSC Ensembl
chr2:61850245..61863695hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3813451
hg1913451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206372
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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