A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989848



Internal ID12629152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145764515..146028515hg38UCSC Ensembl
Innerchr3:145482302..145746302hg19UCSC Ensembl
Innerchr3:146964992..147228992hg18UCSC Ensembl
Innerchr3:146965000..147229000hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38264001
hg19264001
hg18264001
hg17264001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751980
Supporting Variants
SamplesBEC_618
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989848
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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