A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100408



Internal ID21493182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8885593..8885658hg38UCSC Ensembl
chr17:8788910..8788975hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586245
Supporting Variants
SamplesNA19238
Known GenesPIK3R5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100408
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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