A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512034



Internal ID22569986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17447811..17453449hg38UCSC Ensembl
chr9:17447809..17453447hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg385639
hg195639
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863914
Supporting Variants
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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