A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988159



Internal ID12980048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180546560..180556514hg38UCSC Ensembl
Innerchr4:181467713..181477667hg19UCSC Ensembl
Innerchr4:181704707..181714661hg18UCSC Ensembl
Innerchr4:181842862..181852816hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg389955
hg199955
hg189955
hg179955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35033
Supporting Variants
SamplesNA18532
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988159
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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