A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377120



Internal ID22434990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89829649..89831981hg38UCSC Ensembl
chr16:89896057..89898389hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382333
hg192333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931985
Supporting Variants
Samples
Known GenesSPIRE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377120
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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