A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988305



Internal ID12981193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41379305..41466005hg38UCSC Ensembl
Innerchr3:41420796..41507496hg19UCSC Ensembl
Innerchr3:41395800..41482500hg18UCSC Ensembl
Innerchr3:41395800..41482500hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3886701
hg1986701
hg1886701
hg1786701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34828
Supporting Variants
SamplesNA18947
Known GenesULK4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988305
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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