A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892133



Internal ID19186529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9256023..9280461hg38UCSC Ensembl
Outerchr12:9256023..9280461hg38UCSC Ensembl
Innerchr12:9408619..9433057hg19UCSC Ensembl
Outerchr12:9408619..9433057hg19UCSC Ensembl
Innerchr12:9299886..9324324hg18UCSC Ensembl
Outerchr12:9299886..9324324hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3824439
hg1924439
hg1824439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780806
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892133
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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