A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244367



Internal ID21304742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11967033..11975492hg38UCSC Ensembl
Outerchr9:11967011..11978913hg38UCSC Ensembl
Innerchr9:11967033..11975492hg19UCSC Ensembl
Outerchr9:11967011..11978913hg19UCSC Ensembl
Innerchr9:11957033..11965492hg18UCSC Ensembl
Outerchr9:11957011..11968913hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3811903
hg1911903
hg1811903
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesNGO_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244367
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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