A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988838



Internal ID12983385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176789401..176961448hg38UCSC Ensembl
Innerchr3:176507189..176679236hg19UCSC Ensembl
Innerchr3:177989883..178161930hg18UCSC Ensembl
Innerchr3:177989891..178161938hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38172048
hg19172048
hg18172048
hg17172048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751983
Supporting Variants
SamplesSPC_167
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988838
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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