A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14195782



Internal ID3099395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66809016..66810715hg38UCSC Ensembl
Innerchr11:66809027..66810705hg38UCSC Ensembl
Outerchr11:66809006..66810726hg38UCSC Ensembl
chr11:66576487..66578186hg19UCSC Ensembl
Innerchr11:66576498..66578176hg19UCSC Ensembl
Outerchr11:66576477..66578197hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626698
Supporting Variants
SamplesHG02724
Known GenesC11orf80
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14195782
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