A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599645



Internal ID6639908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11416510..11417687hg38UCSC Ensembl
Innerchr4:11416560..11417637hg38UCSC Ensembl
Outerchr4:11416460..11417737hg38UCSC Ensembl
chr4:11418134..11419311hg19UCSC Ensembl
Innerchr4:11418184..11419261hg19UCSC Ensembl
Outerchr4:11418084..11419361hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11357069
SamplesHG02728
Known GenesHS3ST1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599645
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