A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400232



Internal ID21057785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152618998..152632332hg38UCSC Ensembl
chr5:151998558..152011892hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3813335
hg1913335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400232
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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