A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520507



Internal ID20893868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50560912..50573812hg38UCSC Ensembl
chr18:48087282..48100182hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3812901
hg1912901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194148
Samples
Known GenesMAPK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520507
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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