A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984823



Internal ID12636888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3552886..3847206hg38UCSC Ensembl
Innerchr3:3594570..3888890hg19UCSC Ensembl
Innerchr3:3569570..3863890hg18UCSC Ensembl
Innerchr3:3569570..3863890hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38294321
hg19294321
hg18294321
hg17294321
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)essv6984823
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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