A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357566



Internal ID21015119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108591546..108675320hg38UCSC Ensembl
chr3:108310393..108394167hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3883775
hg1983775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093323
Samples
Known GenesDZIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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