A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367652



Internal ID21025205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102866971..102901151hg38UCSC Ensembl
chr3:102585815..102619995hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3834181
hg1934181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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