A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099805



Internal ID21429422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8343293..8344649hg38UCSC Ensembl
chr17:8246611..8247967hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604059
Supporting Variants
SamplesHG00731
Known GenesODF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099805
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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