A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362079



Internal ID21019632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103793268..103801788hg38UCSC Ensembl
chr3:103512112..103520632hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg388521
hg198521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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