A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516816



Internal ID20890177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73146045..73198329hg38UCSC Ensembl
chr18:70813280..70865564hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3852285
hg1952285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197174
Samples
Known GenesLOC400655
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516816
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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