A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612111



Internal ID21804158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47133203..47133372hg38UCSC Ensembl
chr15:47425401..47425570hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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