A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11383328



Internal ID1886395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29939944..29949326hg38UCSC Ensembl
Innerchr4:29939982..29949289hg38UCSC Ensembl
Outerchr4:29939907..29949364hg38UCSC Ensembl
chr4:29941566..29950948hg19UCSC Ensembl
Innerchr4:29941604..29950911hg19UCSC Ensembl
Outerchr4:29941529..29950986hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg389383
hg199383
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600059
Supporting Variants
SamplesHG01776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11383328
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