A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396920



Internal ID21054473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141923016..141925084hg38UCSC Ensembl
chr5:141302581..141304649hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382069
hg192069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213217
Samples
Known GenesKIAA0141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396920
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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