A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984547



Internal ID12977154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26269605..26382005hg38UCSC Ensembl
Innerchr3:26311096..26423496hg19UCSC Ensembl
Innerchr3:26286100..26398500hg18UCSC Ensembl
Innerchr3:26286100..26398500hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38112401
hg19112401
hg18112401
hg17112401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751997
Supporting Variants
SamplesBEC_717
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984547
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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