A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987684



Internal ID12983514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162165510..162298510hg38UCSC Ensembl
Innerchr3:161883298..162016298hg19UCSC Ensembl
Innerchr3:163365992..163498992hg18UCSC Ensembl
Innerchr3:163366000..163499000hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38133001
hg19133001
hg18133001
hg17133001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751981
Supporting Variants
SamplesSPC_18
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987684
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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