A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354479



Internal ID21012032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70155593..70172017hg38UCSC Ensembl
chr2:70382725..70399149hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3816425
hg1916425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206996
Samples
Known GenesC2orf42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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