A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215583



Internal ID20782623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132604434..132995678hg38UCSC Ensembl
chr6:132925573..133316817hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38391245
hg19391245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606163
Supporting Variants
Samples
Known GenesRPS12, SLC18B1, SNORA33, SNORD100, SNORD101, TAAR1, TAAR2, TAAR3, VNN1, VNN2, VNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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