A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523078



Internal ID20896439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69151406..69159843hg38UCSC Ensembl
chr18:66818643..66827080hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg388438
hg198438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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