A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610192



Internal ID21802239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40683217..40683624hg38UCSC Ensembl
chr15:40975415..40975822hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036952
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610192
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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