A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869842



Internal ID22644777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69215745..69237949hg38UCSC Ensembl
chr17:67211886..67234090hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3822205
hg1922205
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475853
Samples
Known GenesABCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869842
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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