A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368176



Internal ID21025729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98806705..98807365hg38UCSC Ensembl
chr3:98525549..98526209hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104950
Samples
Known GenesDCBLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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