A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608675



Internal ID21800722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51914416..51914632hg38UCSC Ensembl
chr15:52206613..52206829hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608675
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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