A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359170



Internal ID21016723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98885887..98901409hg38UCSC Ensembl
chr3:98604731..98620253hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3815523
hg1915523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104953
Samples
Known GenesDCBLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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