A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700047



Internal ID123713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27547752..27549208hg38UCSC Ensembl
chr15:27792898..27794354hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381457
hg191457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700047
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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