A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983729



Internal ID12629142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145764299..146028026hg38UCSC Ensembl
Innerchr3:145482086..145745813hg19UCSC Ensembl
Innerchr3:146964776..147228503hg18UCSC Ensembl
Innerchr3:146964784..147228511hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38263728
hg19263728
hg18263728
hg17263728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751980
Supporting Variants
SamplesBEC_618
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983729
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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