A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984822



Internal ID12636887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3552885..3847210hg38UCSC Ensembl
Innerchr3:3594569..3888894hg19UCSC Ensembl
Innerchr3:3569569..3863894hg18UCSC Ensembl
Innerchr3:3569569..3863894hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38294326
hg19294326
hg18294326
hg17294326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752001
Supporting Variants
SamplesSPC_181
Known GenesLRRN1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984822
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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