A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987830



Internal ID12971765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11262339..11952796hg38UCSC Ensembl
Innerchr9:11262339..11952796hg19UCSC Ensembl
Innerchr9:11252339..11942796hg18UCSC Ensembl
Innerchr9:11252339..11942796hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38690458
hg19690458
hg18690458
hg17690458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752276
Supporting Variants
SamplesBEC_101
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987830
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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