A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615298



Internal ID21807345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43198080..43199968hg38UCSC Ensembl
chr15:43490278..43492166hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032571
Supporting Variants
Samples
Known GenesEPB42
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615298
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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