A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395938



Internal ID21053491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87473982..87611586hg38UCSC Ensembl
chr5:86769799..86907403hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38137605
hg19137605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395938
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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