A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408547



Internal ID21066100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67560665..67568874hg38UCSC Ensembl
chr5:66856493..66864702hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg388210
hg198210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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