A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206954



Internal ID20773994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65253561..65306955hg38UCSC Ensembl
chr2:65480695..65534089hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3853395
hg1953395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353929
Supporting Variants
Samples
Known GenesACTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206954
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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