A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532854



Internal ID20906215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31388130..31472251hg38UCSC Ensembl
chr18:28968093..29052214hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3884122
hg1984122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186385
Samples
Known GenesDSG3, DSG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532854
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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