A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393410



Internal ID21050963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33050414..33050619hg38UCSC Ensembl
chr5:33050520..33050725hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393410
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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