A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529526



Internal ID20902887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78944601..78949263hg38UCSC Ensembl
chr18:76704601..76709263hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg384663
hg194663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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