A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363154



Internal ID21020707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9412586..9417504hg38UCSC Ensembl
chr3:9454270..9459188hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384919
hg194919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106689
Samples
Known GenesSETD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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