A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982184



Internal ID12626633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100580485..100736295hg38UCSC Ensembl
Innerchr3:100299329..100455139hg19UCSC Ensembl
Innerchr3:101782019..101937829hg18UCSC Ensembl
Innerchr3:101782019..101937829hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38155811
hg19155811
hg18155811
hg17155811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751967
Supporting Variants
SamplesBEC_400
Known GenesGPR128, TFG
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982184
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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