A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980058



Internal ID12981191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41364837..41460246hg38UCSC Ensembl
Innerchr3:41406328..41501737hg19UCSC Ensembl
Innerchr3:41381332..41476741hg18UCSC Ensembl
Innerchr3:41381332..41476741hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3895410
hg1995410
hg1895410
hg1795410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34828
Supporting Variants
SamplesNA18947
Known GenesULK4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980058
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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