A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248554



Internal ID21303390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11676182..11967032hg38UCSC Ensembl
Outerchr9:11675235..11967033hg38UCSC Ensembl
Innerchr9:11676182..11967032hg19UCSC Ensembl
Outerchr9:11675235..11967033hg19UCSC Ensembl
Innerchr9:11666182..11957032hg18UCSC Ensembl
Outerchr9:11665235..11957033hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38291799
hg19291799
hg18291799
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesMLY_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248554
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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