A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11641084



Internal ID1655789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145353203..145368955hg38UCSC Ensembl
Innerchr4:145353353..145368805hg38UCSC Ensembl
Outerchr4:145353053..145369105hg38UCSC Ensembl
chr4:146274355..146290107hg19UCSC Ensembl
Innerchr4:146274505..146289957hg19UCSC Ensembl
Outerchr4:146274205..146290257hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3815753
hg1915753
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602559
Supporting Variants
SamplesHG01522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11641084
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