A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489838



Internal ID21147391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59676101..59678800hg38UCSC Ensembl
chr13:60250235..60252934hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010505
Samples
Known GenesDIAPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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