A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365900



Internal ID21023453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132175701..132185000hg38UCSC Ensembl
chr3:131894545..131903844hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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