A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928256



Internal ID22703493
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 Variantsnssv17382968
Samples
Known GenesNTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928256
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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