A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602817



Internal ID6989850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157699145..157722092hg38UCSC Ensembl
Innerchr4:157699645..157721592hg38UCSC Ensembl
Outerchr4:157698145..157723092hg38UCSC Ensembl
chr4:158620297..158643244hg19UCSC Ensembl
Innerchr4:158620797..158642744hg19UCSC Ensembl
Outerchr4:158619297..158644244hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3822948
hg1922948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11660043, essv11660042, essv11660037, essv11660038, essv11660040, essv11660041, essv11660036, essv11660039
SamplesNA19036, NA19347, HG01882, HG03472, HG03085, NA19320, NA19310, NA19096
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602817
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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