A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626047



Internal ID7012881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39695146..39697469hg38UCSC Ensembl
Innerchr11:39695146..39697469hg38UCSC Ensembl
Outerchr11:39694933..39697653hg38UCSC Ensembl
chr11:39716696..39719019hg19UCSC Ensembl
Innerchr11:39716696..39719019hg19UCSC Ensembl
Outerchr11:39716483..39719203hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382324
hg192324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14100704, essv14100703, essv14100706, essv14100698, essv14100701, essv14100697, essv14100696, essv14100700, essv14100707, essv14100699, essv14100709, essv14100708, essv14100702, essv14100694, essv14100695, essv14100705, essv14100693
SamplesNA18998, NA18999, NA19067, NA18944, NA18960, NA18949, NA18970, NA19002, NA18985, NA18973, NA18954, NA19007, NA19006, NA18948, NA19090, NA19080, NA19074
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626047
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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