A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599449



Internal ID21791494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41382984..41383111hg38UCSC Ensembl
chr15:41675182..41675309hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599449
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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