A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411131



Internal ID21068684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81931339..81931990hg38UCSC Ensembl
chr5:81227158..81227809hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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