A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370399



Internal ID21027952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161865395..161865986hg38UCSC Ensembl
chr3:161583183..161583774hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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