A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515642



Internal ID20889003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79565501..79650600hg38UCSC Ensembl
chr18:77325501..77410600hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3885100
hg1985100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3410n223
Supporting Variantsnssv18197265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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