A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094849



Internal ID21431136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105382356..105382664hg38UCSC Ensembl
chr13:106034706..106035014hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590276
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094849
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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