A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080899



Internal ID21461022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14686613..14687174hg38UCSC Ensembl
chr16:14780470..14781031hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595003
Supporting Variants
SamplesHG02818
Known GenesPLA2G10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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