A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852679



Internal ID22627614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17349747..17352954hg38UCSC Ensembl
chr9:17349745..17352952hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg383208
hg193208
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512015
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852679
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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