A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249105



Internal ID21312969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11975493..12078499hg38UCSC Ensembl
Outerchr9:11975492..12082380hg38UCSC Ensembl
Innerchr9:11975493..12078499hg19UCSC Ensembl
Outerchr9:11975492..12082380hg19UCSC Ensembl
Innerchr9:11965493..12068499hg18UCSC Ensembl
Outerchr9:11965492..12072380hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38106889
hg19106889
hg18106889
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesSNI_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249105
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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