A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608778



Internal ID21800825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87125275..87125362hg38UCSC Ensembl
chr15:87668506..87668593hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608778
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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