A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986095



Internal ID12626641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100639466..100709466hg38UCSC Ensembl
Innerchr3:100358310..100428310hg19UCSC Ensembl
Innerchr3:101841000..101911000hg18UCSC Ensembl
Innerchr3:101841000..101911000hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3870001
hg1970001
hg1870001
hg1770001
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986095
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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