A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372962



Internal ID21030515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153270398..153279027hg38UCSC Ensembl
chr3:152988187..152996816hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg388630
hg198630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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