A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990134



Internal ID12637259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13321602..13396813hg38UCSC Ensembl
Innerchr9:13321601..13396812hg19UCSC Ensembl
Innerchr9:13311601..13386812hg18UCSC Ensembl
Innerchr9:13311601..13386812hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3875212
hg1975212
hg1875212
hg1775212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752281
Supporting Variants
SamplesSPC_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990134
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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