A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250874



Internal ID21305760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11701596..11887372hg38UCSC Ensembl
Outerchr9:11698909..11895122hg38UCSC Ensembl
Innerchr9:11701596..11887372hg19UCSC Ensembl
Outerchr9:11698909..11895122hg19UCSC Ensembl
Innerchr9:11691596..11877372hg18UCSC Ensembl
Outerchr9:11688909..11885122hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38196214
hg19196214
hg18196214
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesNGO_23
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250874
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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