A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984706



Internal ID12983374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176850510..176927510hg38UCSC Ensembl
Innerchr3:176568298..176645298hg19UCSC Ensembl
Innerchr3:178050992..178127992hg18UCSC Ensembl
Innerchr3:178051000..178128000hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3877001
hg1977001
hg1877001
hg1777001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751983
Supporting Variants
SamplesSPC_167
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984706
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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