A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373370



Internal ID22599039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9111179..9119430hg38UCSC Ensembl
chr17:9014496..9022747hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg388252
hg198252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938973
Supporting Variants
Samples
Known GenesNTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373370
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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