A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980359



Internal ID12978246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7292836..7781365hg38UCSC Ensembl
Innerchr9:7292836..7781365hg19UCSC Ensembl
Innerchr9:7282836..7771365hg18UCSC Ensembl
Innerchr9:7282836..7771365hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38488530
hg19488530
hg18488530
hg17488530
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)essv6980359
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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