A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523980



Internal ID20897341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74515041..74684167hg38UCSC Ensembl
chr18:72182276..72396123hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38169127
hg19213848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197191
Samples
Known GenesCNDP1, CNDP2, LINC00909, ZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523980
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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