A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360192



Internal ID21017745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96771293..96786903hg38UCSC Ensembl
chr3:96490137..96505747hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3815611
hg1915611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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