A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779545



Internal ID18825190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:13384904..13409588hg38UCSC Ensembl
Innerchr12:13537838..13562522hg19UCSC Ensembl
Innerchr12:13429105..13453789hg18UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3824685
hg1924685
hg1824685
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892145
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779545
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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