A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399128



Internal ID21056681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164294921..167231615hg38UCSC Ensembl
chr5:163721927..166658620hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382936695
hg192936694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127590
Samples
Known GenesLOC101927835, LOC102546299, LOC102557615
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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