A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094415



Internal ID21431274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11638052..11638113hg38UCSC Ensembl
chr16:11731908..11731969hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596117
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094415
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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