A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216797



Internal ID20783837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109567216..109604397hg38UCSC Ensembl
chr6:109888419..109925600hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3837182
hg1937182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610140
Supporting Variants
Samples
Known GenesAK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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