A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603433



Internal ID6990464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183086909..183088656hg38UCSC Ensembl
Innerchr4:183086909..183088656hg38UCSC Ensembl
Outerchr4:183086635..183088917hg38UCSC Ensembl
chr4:184008062..184009809hg19UCSC Ensembl
Innerchr4:184008062..184009809hg19UCSC Ensembl
Outerchr4:184007788..184010070hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11732281, essv11732275, essv11732279, essv11732280, essv11732276, essv11732284, essv11732272, essv11732274, essv11732271, essv11732270, essv11732278, essv11732277, essv11732273, essv11732283, essv11732282
SamplesHG00542, HG00536, NA18979, HG00457, NA18959, NA19005, NA18940, HG03796, HG00534, NA18539, HG02164, HG00500, HG00684, NA18564, NA18965
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603433
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer