A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603486



Internal ID6990517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185084420..185086370hg38UCSC Ensembl
Innerchr4:185084448..185086342hg38UCSC Ensembl
Outerchr4:185084392..185086398hg38UCSC Ensembl
chr4:186005574..186007524hg19UCSC Ensembl
Innerchr4:186005602..186007496hg19UCSC Ensembl
Outerchr4:186005546..186007552hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381951
hg191951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11735917
SamplesNA19461
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603486
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