A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987856



Internal ID12982118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12287871..12572122hg38UCSC Ensembl
Innerchr9:12287871..12572122hg19UCSC Ensembl
Innerchr9:12277871..12562122hg18UCSC Ensembl
Innerchr9:12277871..12562122hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38284252
hg19284252
hg18284252
hg17284252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34901
Supporting Variants
SamplesNA19130
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987856
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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