A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484106



Internal ID21141659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51361025..51361748hg38UCSC Ensembl
chr13:51935161..51935884hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009665
Samples
Known GenesINTS6, SERPINE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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