A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892247



Internal ID19183067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95625342..95632203hg38UCSC Ensembl
Outerchr12:95625342..95632203hg38UCSC Ensembl
Innerchr12:96019118..96025979hg19UCSC Ensembl
Outerchr12:96019118..96025979hg19UCSC Ensembl
Innerchr12:94543249..94550110hg18UCSC Ensembl
Outerchr12:94543249..94550110hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg386862
hg196862
hg186862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785329
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892247
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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