A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526463



Internal ID20899824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74357992..74374131hg38UCSC Ensembl
chr18:72025227..72041366hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3816140
hg1916140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197188
Samples
Known GenesC18orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526463
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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