A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486439



Internal ID21143992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72776263..72781638hg38UCSC Ensembl
chr13:73350401..73355776hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg385376
hg195376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012805
Samples
Known GenesDIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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