A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523955



Internal ID20897316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45815434..45846162hg38UCSC Ensembl
chr18:43395399..43426127hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3830729
hg1930729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188135
Samples
Known GenesSIGLEC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523955
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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