A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371019



Internal ID22596688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10688818..10689133hg38UCSC Ensembl
chr17:10592135..10592450hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935732
Supporting Variants
Samples
Known GenesSCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371019
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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