A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3630496



Internal ID7017313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98038052..98042532hg38UCSC Ensembl
Innerchr12:98038060..98042524hg38UCSC Ensembl
Outerchr12:98038044..98042540hg38UCSC Ensembl
chr12:98431830..98436310hg19UCSC Ensembl
Innerchr12:98431838..98436302hg19UCSC Ensembl
Outerchr12:98431822..98436318hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg384481
hg194481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14584600
SamplesHG00341
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3630496
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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