A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359889



Internal ID21017442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153794501..153802400hg38UCSC Ensembl
chr3:153512290..153520189hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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