A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360935



Internal ID21018488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32833483..32836247hg38UCSC Ensembl
chr3:32874975..32877739hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382765
hg192765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099426
Samples
Known GenesTRIM71
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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