A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604232



Internal ID21796279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56027303..56027483hg38UCSC Ensembl
chr15:56319501..56319681hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604232
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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