A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515691



Internal ID20889052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68478987..68599450hg38UCSC Ensembl
chr18:66146224..66266687hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38120464
hg19120464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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