A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086478



Internal ID21491112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88009812..88009873hg38UCSC Ensembl
chr16:88043418..88043479hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596591
Supporting Variants
SamplesNA19238
Known GenesBANP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086478
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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