A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087697



Internal ID21458070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94501974..94502077hg38UCSC Ensembl
chr13:95154228..95154331hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594783
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087697
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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