A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602845



Internal ID6989878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159389896..159391660hg38UCSC Ensembl
Innerchr4:159389905..159391651hg38UCSC Ensembl
Outerchr4:159389887..159391669hg38UCSC Ensembl
chr4:160311048..160312812hg19UCSC Ensembl
Innerchr4:160311057..160312803hg19UCSC Ensembl
Outerchr4:160311039..160312821hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11661824, essv11661823
SamplesNA19058, NA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602845
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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