A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626001



Internal ID7012835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38024351..38078424hg38UCSC Ensembl
Innerchr11:38024851..38077924hg38UCSC Ensembl
Outerchr11:38023351..38079424hg38UCSC Ensembl
chr11:38045901..38099974hg19UCSC Ensembl
Innerchr11:38046401..38099474hg19UCSC Ensembl
Outerchr11:38044901..38100974hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3854074
hg1954074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14095084, essv14095085
SamplesHG03782, NA20775
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626001
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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