A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893791



Internal ID18837925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763820..155772524hg38UCSC Ensembl
Outerchr3:155763820..155776126hg38UCSC Ensembl
Innerchr3:155481609..155490313hg19UCSC Ensembl
Outerchr3:155481609..155493915hg19UCSC Ensembl
Innerchr3:156964303..156973007hg18UCSC Ensembl
Outerchr3:156964303..156976609hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3812307
hg1912307
hg1812307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781721, essv25781778
Samples
Known GenesC3orf33
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893791
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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