A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530476



Internal ID20903837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46829167..46829582hg38UCSC Ensembl
chr18:44409130..44409545hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041933
Samples
Known GenesPIAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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