A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981255



Internal ID12973070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7063099..7131315hg38UCSC Ensembl
Innerchr3:7104786..7173002hg19UCSC Ensembl
Innerchr3:7079786..7148002hg18UCSC Ensembl
Innerchr3:7079786..7148002hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3868217
hg1968217
hg1868217
hg1768217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752015
Supporting Variants
SamplesBEC_374
Known GenesGRM7
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981255
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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