A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893726



Internal ID19184546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:76794089..76861784hg38UCSC Ensembl
Outerchr3:76794089..76861784hg38UCSC Ensembl
Innerchr3:76843240..76910935hg19UCSC Ensembl
Outerchr3:76843240..76910935hg19UCSC Ensembl
Innerchr3:76925930..76993625hg18UCSC Ensembl
Outerchr3:76925930..76993625hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3867696
hg1967696
hg1867696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781539
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893726
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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