A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784826



Internal ID19181499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57419153..57508411hg38UCSC Ensembl
Innerchr3:57404880..57494138hg19UCSC Ensembl
Innerchr3:57379920..57469178hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3889259
hg1989259
hg1889259
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893699
Supporting Variants
Samples
Known GenesDNAH12
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784826
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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