A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359763



Internal ID21017316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39078954..39112246hg38UCSC Ensembl
chr3:39120445..39153737hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3833293
hg1933293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211203
Samples
Known GenesGORASP1, TTC21A, WDR48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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