A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982146



Internal ID12626588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100635326..100743683hg38UCSC Ensembl
Innerchr3:100354170..100462527hg19UCSC Ensembl
Innerchr3:101836860..101945217hg18UCSC Ensembl
Innerchr3:101836860..101945217hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38108358
hg19108358
hg18108358
hg17108358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751965
Supporting Variants
SamplesBEC_396
Known GenesGPR128, TFG
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982146
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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