A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516997



Internal ID20890358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38699432..38700123hg38UCSC Ensembl
chr18:36279396..36280087hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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