A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367039



Internal ID21024592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106061740..106062384hg38UCSC Ensembl
chr3:105780587..105781231hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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