A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625912



Internal ID6666060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34476653..34498139hg38UCSC Ensembl
Innerchr11:34476653..34498139hg38UCSC Ensembl
Outerchr11:34476153..34498639hg38UCSC Ensembl
chr11:34498200..34519686hg19UCSC Ensembl
Innerchr11:34498200..34519686hg19UCSC Ensembl
Outerchr11:34497700..34520186hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821487
hg1921487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14089287
SamplesHG03432
Known GenesELF5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625912
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