A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026322



Internal ID20593362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69811044..69817255hg38UCSC Ensembl
chr15:70103383..70109594hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386212
hg196212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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