A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984808



Internal ID12983547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66759594..66830898hg38UCSC Ensembl
Innerchr3:66810018..66881322hg19UCSC Ensembl
Innerchr3:66892708..66964012hg18UCSC Ensembl
Innerchr3:66892708..66964012hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3871305
hg1971305
hg1871305
hg1771305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752013
Supporting Variants
SamplesSPC_180
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984808
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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