A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984771



Internal ID12983470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75343222..75705553hg38UCSC Ensembl
Innerchr3:75392373..75754704hg19UCSC Ensembl
Innerchr3:75475063..75837394hg18UCSC Ensembl
Innerchr3:75475063..75837394hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38362332
hg19362332
hg18362332
hg17362332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752017
Supporting Variants
SamplesSPC_178
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984771
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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