A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512569



Internal ID22570523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27221693..27225241hg38UCSC Ensembl
chr9:27221691..27225239hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg383549
hg193549
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859387
Supporting Variants
Samples
Known GenesTEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512569
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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