A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512033



Internal ID22569985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17441889..17447910hg38UCSC Ensembl
chr9:17441887..17447908hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg386022
hg196022
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861492
Supporting Variants
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512033
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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