A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395953



Internal ID21053506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77545978..77571418hg38UCSC Ensembl
chr5:76841803..76867243hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3825441
hg1925441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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