A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375367



Internal ID21032920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106883344..106917381hg38UCSC Ensembl
chr3:106602191..106636228hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3834038
hg1934038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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