A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486155



Internal ID21143708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48096836..48100992hg38UCSC Ensembl
chr13:48670972..48675128hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg384157
hg194157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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