A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984819



Internal ID12636884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3539056..3858106hg38UCSC Ensembl
Innerchr3:3580740..3899790hg19UCSC Ensembl
Innerchr3:3555740..3874790hg18UCSC Ensembl
Innerchr3:3555740..3874790hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38319051
hg19319051
hg18319051
hg17319051
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984819
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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