A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787075



Internal ID19182964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:55034228..55055047hg38UCSC Ensembl
Innerchr3:55068255..55089074hg19UCSC Ensembl
Innerchr3:55043295..55064114hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3820820
hg1920820
hg1820820
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893698
Supporting Variants
Samples
Known GenesCACNA2D3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787075
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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