A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355359



Internal ID21012912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64839344..64842513hg38UCSC Ensembl
chr2:65066478..65069647hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383170
hg193170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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