A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980361



Internal ID12978263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7368850..7595560hg38UCSC Ensembl
Innerchr9:7368850..7595560hg19UCSC Ensembl
Innerchr9:7358850..7585560hg18UCSC Ensembl
Innerchr9:7358850..7585560hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38226711
hg19226711
hg18226711
hg17226711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34566
Supporting Variants
SamplesNA07345
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980361
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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