A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518030



Internal ID20891391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31401327..31401820hg38UCSC Ensembl
chr18:28981290..28981783hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039921
Samples
Known GenesDSG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518030
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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