A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398118



Internal ID21055671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159967853..159968273hg38UCSC Ensembl
chr5:159394860..159395280hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215926
Samples
Known GenesADRA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398118
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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