A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14095120



Internal ID2599430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38105178..38112680hg38UCSC Ensembl
Innerchr11:38105228..38112630hg38UCSC Ensembl
Outerchr11:38105102..38112756hg38UCSC Ensembl
chr11:38126728..38134230hg19UCSC Ensembl
Innerchr11:38126778..38134180hg19UCSC Ensembl
Outerchr11:38126652..38134306hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387503
hg197503
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626004
Supporting Variants
SamplesHG02304
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14095120
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