A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234919



Internal ID20801959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33883982..33937288hg38UCSC Ensembl
chr6:33851759..33905065hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3853307
hg1953307
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413818
Supporting Variants
Samples
Known GenesLINC01016, MIR7159
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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