A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14178523



Internal ID2438046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61940264..61941576hg38UCSC Ensembl
Innerchr11:61940294..61941547hg38UCSC Ensembl
Outerchr11:61940235..61941606hg38UCSC Ensembl
chr11:61707736..61709048hg19UCSC Ensembl
Innerchr11:61707766..61709019hg19UCSC Ensembl
Outerchr11:61707707..61709078hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626587
Supporting Variants
SamplesHG02150
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14178523
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