A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517774



Internal ID20891135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36155902..36156997hg38UCSC Ensembl
chr18:33735865..33736960hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184312
Samples
Known GenesELP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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