A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247577



Internal ID21311067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27230511..27252787hg38UCSC Ensembl
Outerchr9:27230154..27257584hg38UCSC Ensembl
Innerchr9:27230509..27252785hg19UCSC Ensembl
Outerchr9:27230152..27257582hg19UCSC Ensembl
Innerchr9:27220509..27242785hg18UCSC Ensembl
Outerchr9:27220152..27247582hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3827431
hg1927431
hg1827431
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169847
Supporting Variants
SamplesPML_3
Known GenesLINC00032, TEK
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247577
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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