A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989343



Internal ID12974787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75344579..75726932hg38UCSC Ensembl
Innerchr3:75393730..75776083hg19UCSC Ensembl
Innerchr3:75476420..75858773hg18UCSC Ensembl
Innerchr3:75476420..75858773hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38382354
hg19382354
hg18382354
hg17382354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752018
Supporting Variants
SamplesBEC_540
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)essv6989343
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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