A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529852



Internal ID20903213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8930279..8941330hg38UCSC Ensembl
chr18:8930277..8941328hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3811052
hg1911052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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