A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412449



Internal ID21070002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132992900..132995632hg38UCSC Ensembl
chr5:132328592..132331324hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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