A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363355



Internal ID21020908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52536290..52542700hg38UCSC Ensembl
chr3:52570306..52576716hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg386411
hg196411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209990
Samples
Known GenesSMIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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