A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989928



Internal ID12977828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30361740..30661614hg38UCSC Ensembl
Innerchr9:30361738..30661612hg19UCSC Ensembl
Innerchr9:30351738..30651612hg18UCSC Ensembl
Innerchr9:30351738..30651612hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38299875
hg19299875
hg18299875
hg17299875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752298
Supporting Variants
SamplesBEC_799
Known GenesLOC401497
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989928
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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