A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251507



Internal ID21312472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10744135..10756722hg38UCSC Ensembl
Outerchr9:10743871..10764097hg38UCSC Ensembl
Innerchr9:10744135..10756722hg19UCSC Ensembl
Outerchr9:10743871..10764097hg19UCSC Ensembl
Innerchr9:10734135..10746722hg18UCSC Ensembl
Outerchr9:10733871..10754097hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3820227
hg1920227
hg1820227
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169379
Supporting Variants
SamplesSNI_2
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251507
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