A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989153



Internal ID12981380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104727466..104955466hg38UCSC Ensembl
Innerchr3:104446310..104674310hg19UCSC Ensembl
Innerchr3:105929000..106157000hg18UCSC Ensembl
Innerchr3:105929000..106157000hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38228001
hg19228001
hg18228001
hg17228001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35023
Supporting Variants
SamplesNA18966
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989153
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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