A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184824



Internal ID20751864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50357685..50358301hg38UCSC Ensembl
chr15:50649882..50650498hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497100
Supporting Variants
Samples
Known GenesGABPB1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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