A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181260



Internal ID20748300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46635986..46669617hg38UCSC Ensembl
chr15:46928184..46961815hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3833632
hg1933632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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