A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405196



Internal ID21062749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141605260..141606460hg38UCSC Ensembl
chr5:140984827..140986027hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213213
Samples
Known GenesDIAPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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