A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251115



Internal ID21304951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12082380..12137134hg38UCSC Ensembl
Outerchr9:12078499..12139379hg38UCSC Ensembl
Innerchr9:12082380..12137134hg19UCSC Ensembl
Outerchr9:12078499..12139379hg19UCSC Ensembl
Innerchr9:12072380..12127134hg18UCSC Ensembl
Outerchr9:12068499..12129379hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3860881
hg1960881
hg1860881
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesNGO_17
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251115
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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