A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359041



Internal ID21016594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112773119..112780506hg38UCSC Ensembl
chr3:112491966..112499353hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg387388
hg197388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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