A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089377



Internal ID21464532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44681898..44683622hg38UCSC Ensembl
chr13:45256034..45257758hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg381725
hg191725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599832
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089377
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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