A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247450



Internal ID21311765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11975493..12074207hg38UCSC Ensembl
Outerchr9:11975492..12077080hg38UCSC Ensembl
Innerchr9:11975493..12074207hg19UCSC Ensembl
Outerchr9:11975492..12077080hg19UCSC Ensembl
Innerchr9:11965493..12064207hg18UCSC Ensembl
Outerchr9:11965492..12067080hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38101589
hg19101589
hg18101589
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)nssv14247450
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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