A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372010



Internal ID21029563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137874437..137884133hg38UCSC Ensembl
chr3:137593279..137602975hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg389697
hg199697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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