A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798320



Internal ID19181906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10522696..10545656hg38UCSC Ensembl
Innerchr12:10675295..10698255hg19UCSC Ensembl
Innerchr12:10566562..10589522hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3822961
hg1922961
hg1822961
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892139
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798320
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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