A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628063



Internal ID7014888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129320016..129320762hg38UCSC Ensembl
Innerchr11:129320038..129320740hg38UCSC Ensembl
Outerchr11:129319994..129320784hg38UCSC Ensembl
chr11:129189911..129190657hg19UCSC Ensembl
Innerchr11:129189933..129190635hg19UCSC Ensembl
Outerchr11:129189889..129190679hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14310157
SamplesHG00105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628063
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