A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220372



Internal ID20787412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40345948..40352908hg38UCSC Ensembl
chr6:40313687..40320647hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg386961
hg196961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410795
Supporting Variants
Samples
Known GenesLINC00951
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220372
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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