A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367262



Internal ID21024815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56717042..56723614hg38UCSC Ensembl
chr3:56751070..56757642hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg386573
hg196573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367262
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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