A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981532



Internal ID12972279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11236474..11538142hg38UCSC Ensembl
Innerchr9:11236474..11538142hg19UCSC Ensembl
Innerchr9:11226474..11528142hg18UCSC Ensembl
Innerchr9:11226474..11528142hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38301669
hg19301669
hg18301669
hg17301669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752275
Supporting Variants
SamplesBEC_293
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981532
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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