A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387903



Internal ID22445773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59488719..59489007hg38UCSC Ensembl
chr15:59780918..59781206hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932649
Supporting Variants
Samples
Known GenesFAM81A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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