A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097641



Internal ID21411274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26372078..26372410hg38UCSC Ensembl
chr16:26383399..26383731hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591281
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097641
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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