A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879344



Internal ID22654313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70106695..70108344hg38UCSC Ensembl
chr17:68102836..68104485hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475863
Samples
Known GenesKCNJ16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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