A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244519



Internal ID21304612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73405942..73411750hg38UCSC Ensembl
Outerchr9:73398521..73413807hg38UCSC Ensembl
Innerchr9:76020858..76026666hg19UCSC Ensembl
Outerchr9:76013437..76028723hg19UCSC Ensembl
Innerchr9:75210678..75216486hg18UCSC Ensembl
Outerchr9:75203257..75218543hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3815287
hg1915287
hg1815287
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169365
Supporting Variants
SamplesNGO_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244519
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer