A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369663



Internal ID21027216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63809642..63842615hg38UCSC Ensembl
chr3:63795318..63828291hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3832974
hg1932974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212950
Samples
Known GenesC3orf49, THOC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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