A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989902



Internal ID12977585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19786640..20125181hg38UCSC Ensembl
Innerchr4:19788263..20126804hg19UCSC Ensembl
Innerchr4:19397361..19735902hg18UCSC Ensembl
Innerchr4:19464532..19803073hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38338542
hg19338542
hg18338542
hg17338542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752044
Supporting Variants
SamplesBEC_758
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989902
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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