A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526915



Internal ID20900276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75618621..75639396hg38UCSC Ensembl
chr18:73330576..73351351hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3820776
hg1920776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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