A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530672



Internal ID20904033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71077563..71141638hg38UCSC Ensembl
chr18:68744799..68808874hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3864076
hg1964076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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