A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524839



Internal ID20898200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24474883..24482125hg38UCSC Ensembl
chr18:22054847..22062089hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg387243
hg197243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192083
Samples
Known GenesHRH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524839
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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