A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100001



Internal ID21486964
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 StatusS
Merged Variantsnsv5585169
Supporting Variants
SamplesNA12878
Known GenesNTN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100001
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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