A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362165



Internal ID21019718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49221384..49229063hg38UCSC Ensembl
chr3:49258817..49266496hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg387680
hg197680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209354
Samples
Known GenesCCDC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362165
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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