A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519375



Internal ID20892736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30999176..30999544hg38UCSC Ensembl
chr18:28579142..28579510hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039886
Samples
Known GenesDSC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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