A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373575



Internal ID21031128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9873569..9877177hg38UCSC Ensembl
chr3:9915253..9918861hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg383609
hg193609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104947
Samples
Known GenesCIDEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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