A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548603



Internal ID18402993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:757926..765263hg38UCSC Ensembl
Outerchr12:756648..766334hg38UCSC Ensembl
Innerchr12:867092..874429hg19UCSC Ensembl
Outerchr12:865814..875500hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg389687
hg199687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747350
Samples
Known GenesWNK1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548603
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer