A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380773



Internal ID21038326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:30659465..30729484hg38UCSC Ensembl
chr5:30659572..30729591hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3870020
hg1970020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380773
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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