A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247581



Internal ID21307144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10744135..10764097hg38UCSC Ensembl
Outerchr9:10743871..10770064hg38UCSC Ensembl
Innerchr9:10744135..10764097hg19UCSC Ensembl
Outerchr9:10743871..10770064hg19UCSC Ensembl
Innerchr9:10734135..10754097hg18UCSC Ensembl
Outerchr9:10733871..10760064hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3826194
hg1926194
hg1826194
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169379
Supporting Variants
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247581
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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