A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248776



Internal ID21302109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3601355..3618770hg38UCSC Ensembl
Outerchr9:3599252..3625766hg38UCSC Ensembl
Innerchr9:3601355..3618770hg19UCSC Ensembl
Outerchr9:3599252..3625766hg19UCSC Ensembl
Innerchr9:3591355..3608770hg18UCSC Ensembl
Outerchr9:3589252..3615766hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3826515
hg1926515
hg1826515
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170186
Supporting Variants
SamplesMLY_12
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248776
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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