A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092408



Internal ID21477239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24250444..24251915hg38UCSC Ensembl
chr16:24261765..24263236hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381472
hg191472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602526
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092408
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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