A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865409



Internal ID22640344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17386732..17399315hg38UCSC Ensembl
chr9:17386730..17399313hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3812584
hg1912584
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512023
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865409
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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