A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585169



Internal ID21533714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9161898..9162014hg38UCSC Ensembl
chr17:9065215..9065331hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100001
SamplesNA12878
Known GenesNTN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585169
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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