A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11360353



Internal ID2383855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16292366..16302027hg38UCSC Ensembl
Innerchr4:16292400..16301994hg38UCSC Ensembl
Outerchr4:16292333..16302061hg38UCSC Ensembl
chr4:16293989..16303650hg19UCSC Ensembl
Innerchr4:16294023..16303617hg19UCSC Ensembl
Outerchr4:16293956..16303684hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg389662
hg199662
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599751
Supporting Variants
SamplesHG02111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11360353
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