A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191345



Internal ID20758386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84626384..84627758hg38UCSC Ensembl
chr15:85169615..85170989hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381375
hg191375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509267
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191345
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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