A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370569



Internal ID21028122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62100887..62109447hg38UCSC Ensembl
chr3:62086561..62095121hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg388561
hg198561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212933
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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