A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989957



Internal ID12976954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28186823..28380169hg38UCSC Ensembl
Innerchr9:28186821..28380167hg19UCSC Ensembl
Innerchr9:28176821..28370167hg18UCSC Ensembl
Innerchr9:28176821..28370167hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38193347
hg19193347
hg18193347
hg17193347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752293
Supporting Variants
SamplesBEC_704
Known GenesLINGO2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989957
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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