A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093647



Internal ID21401536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35128997..35129224hg38UCSC Ensembl
chr13:35703134..35703361hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598000
Supporting Variants
SamplesHG00096
Known GenesNBEA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093647
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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