A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217121



Internal ID20784161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151469376..151481946hg38UCSC Ensembl
chr6:151790511..151803081hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3812571
hg1912571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617098
Supporting Variants
Samples
Known GenesC6orf211
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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