A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479520



Internal ID22537422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9111136..9119069hg38UCSC Ensembl
chr17:9014453..9022386hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387934
hg197934
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882289
Supporting Variants
Samples
Known GenesNTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479520
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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