A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214531



Internal ID20781572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116586080..116597205hg38UCSC Ensembl
chr6:116907243..116918368hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3811126
hg1911126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606277
Supporting Variants
Samples
Known GenesRWDD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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