A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247563



Internal ID21303647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11835950..12101436hg38UCSC Ensembl
Outerchr9:11825907..12101848hg38UCSC Ensembl
Innerchr9:11835950..12101436hg19UCSC Ensembl
Outerchr9:11825907..12101848hg19UCSC Ensembl
Innerchr9:11825950..12091436hg18UCSC Ensembl
Outerchr9:11815907..12091848hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38275942
hg19275942
hg18275942
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169446
Supporting Variants
SamplesMLY_8
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247563
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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