A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409330



Internal ID21066883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162396230..162400739hg38UCSC Ensembl
chr5:161823236..161827745hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384510
hg194510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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