A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520676



Internal ID20894037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76194575..76195236hg38UCSC Ensembl
chr18:73906530..73907191hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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