A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893699



Internal ID19184519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57426900..57493075hg38UCSC Ensembl
Outerchr3:57419153..57508411hg38UCSC Ensembl
Innerchr3:57412627..57478802hg19UCSC Ensembl
Outerchr3:57404880..57494138hg19UCSC Ensembl
Innerchr3:57387667..57453842hg18UCSC Ensembl
Outerchr3:57379920..57469178hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3889259
hg1989259
hg1889259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784631, essv25784826
Samples
Known GenesDNAH12
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893699
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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