A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980948



Internal ID12982322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30255387..30389495hg38UCSC Ensembl
Innerchr9:30255385..30389493hg19UCSC Ensembl
Innerchr9:30245385..30379493hg18UCSC Ensembl
Innerchr9:30245385..30379493hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38134109
hg19134109
hg18134109
hg17134109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35141
Supporting Variants
SamplesNA19152
Known GenesLOC401497
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980948
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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