A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603816



Internal ID21795863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76340033..76340244hg38UCSC Ensembl
chr15:76632374..76632585hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036522
Supporting Variants
Samples
Known GenesISL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603816
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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