A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11379939



Internal ID4156347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28927556..28933518hg38UCSC Ensembl
Innerchr4:28927574..28933500hg38UCSC Ensembl
Outerchr4:28927538..28933536hg38UCSC Ensembl
chr4:28929178..28935140hg19UCSC Ensembl
Innerchr4:28929196..28935122hg19UCSC Ensembl
Outerchr4:28929160..28935158hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg385963
hg195963
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600030
Supporting Variants
SamplesHG03760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11379939
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