A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11642156



Internal ID5324229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145832703..145838215hg38UCSC Ensembl
Innerchr4:145832753..145838165hg38UCSC Ensembl
Outerchr4:145832653..145838265hg38UCSC Ensembl
chr4:146753855..146759367hg19UCSC Ensembl
Innerchr4:146753905..146759317hg19UCSC Ensembl
Outerchr4:146753805..146759417hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg385513
hg195513
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602566
Supporting Variants
SamplesNA18868
Known GenesZNF827
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11642156
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