A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601781



Internal ID6988817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111501682..111505078hg38UCSC Ensembl
Innerchr4:111501682..111505078hg38UCSC Ensembl
Outerchr4:111501333..111505407hg38UCSC Ensembl
chr4:112422838..112426234hg19UCSC Ensembl
Innerchr4:112422838..112426234hg19UCSC Ensembl
Outerchr4:112422489..112426563hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383397
hg193397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11562580, essv11562583, essv11562581, essv11562582
SamplesNA18621, HG00436, HG02657, NA18622
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601781
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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