A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195776



Internal ID20762816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48321974..48347244hg38UCSC Ensembl
chr15:48614171..48639441hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3825271
hg1925271
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502580
Supporting Variants
Samples
Known GenesDUT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195776
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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