A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614817



Internal ID21806864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36306749..36306801hg38UCSC Ensembl
chr15:36598950..36599002hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614817
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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