A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242118



Internal ID21302993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88992954..89010320hg38UCSC Ensembl
Outerchr9:88989090..89012938hg38UCSC Ensembl
Innerchr9:91607869..91625235hg19UCSC Ensembl
Outerchr9:91604005..91627853hg19UCSC Ensembl
Innerchr9:90797689..90815055hg18UCSC Ensembl
Outerchr9:90793825..90817673hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3823849
hg1923849
hg1823849
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169426
Supporting Variants
SamplesMLY_3
Known GenesC9orf47, S1PR3, SHC3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242118
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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