A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11655746



Internal ID771201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153369645..153372444hg38UCSC Ensembl
Innerchr4:153369646..153372444hg38UCSC Ensembl
Outerchr4:153369645..153372445hg38UCSC Ensembl
chr4:154290797..154293596hg19UCSC Ensembl
Innerchr4:154290798..154293596hg19UCSC Ensembl
Outerchr4:154290797..154293597hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602723
Supporting Variants
SamplesHG00365
Known GenesMND1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11655746
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