A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600030



Internal ID6987074
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11379939
SamplesHG03760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600030
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