A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528695



Internal ID20902056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63415955..63477970hg38UCSC Ensembl
chr18:61083188..61145203hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3862016
hg1962016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184024
Samples
Known GenesSERPINB5, VPS4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528695
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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