A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352785



Internal ID21010338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135688..172022hg38UCSC Ensembl
chr3:177371..213705hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3836335
hg1936335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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