A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475863



Internal ID22533761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70106695..70108344hg38UCSC Ensembl
chr17:68102836..68104485hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879344
Supporting Variants
Samples
Known GenesKCNJ16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475863
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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