A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250959



Internal ID21306116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12061324..12174190hg38UCSC Ensembl
Outerchr9:12056342..12180135hg38UCSC Ensembl
Innerchr9:12061324..12174190hg19UCSC Ensembl
Outerchr9:12056342..12180135hg19UCSC Ensembl
Innerchr9:12051324..12164190hg18UCSC Ensembl
Outerchr9:12046342..12170135hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38123794
hg19123794
hg18123794
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesNGO_25
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250959
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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