A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359204



Internal ID21016757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49196747..49201126hg38UCSC Ensembl
chr3:49234180..49238559hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384380
hg194380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209351
Samples
Known GenesCCDC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359204
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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