A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246109



Internal ID21303918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11926107..11967032hg38UCSC Ensembl
Outerchr9:11922842..11967033hg38UCSC Ensembl
Innerchr9:11926107..11967032hg19UCSC Ensembl
Outerchr9:11922842..11967033hg19UCSC Ensembl
Innerchr9:11916107..11957032hg18UCSC Ensembl
Outerchr9:11912842..11957033hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3844192
hg1944192
hg1844192
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesNGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246109
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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