A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409065



Internal ID21066618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163237778..163244572hg38UCSC Ensembl
chr5:162664784..162671578hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg386795
hg196795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409065
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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