A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600286



Internal ID6987330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39539406..39544119hg38UCSC Ensembl
Innerchr4:39539406..39544119hg38UCSC Ensembl
Outerchr4:39539162..39544369hg38UCSC Ensembl
chr4:39541026..39545739hg19UCSC Ensembl
Innerchr4:39541026..39545739hg19UCSC Ensembl
Outerchr4:39540782..39545989hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384714
hg194714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11401380
SamplesHG03708
Known GenesMIR1273H, UGDH-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600286
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