A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611438



Internal ID21803485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47227880..47228117hg38UCSC Ensembl
chr15:47520077..47520314hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031365
Supporting Variants
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611438
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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