A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244948



Internal ID21311870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11934111..11967032hg38UCSC Ensembl
Outerchr9:11929890..11967033hg38UCSC Ensembl
Innerchr9:11934111..11967032hg19UCSC Ensembl
Outerchr9:11929890..11967033hg19UCSC Ensembl
Innerchr9:11924111..11957032hg18UCSC Ensembl
Outerchr9:11919890..11957033hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3837144
hg1937144
hg1837144
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesSNI_13
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244948
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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