A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405075



Internal ID21062628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106289193..106335577hg38UCSC Ensembl
chr5:105624894..105671278hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3846385
hg1946385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5876n223
Supporting Variantsnssv18123514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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