A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663837



Internal ID9929942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153304529..153312748hg38UCSC Ensembl
Outerchr5:153304492..153312798hg38UCSC Ensembl
Innerchr5:152684089..152692308hg19UCSC Ensembl
Outerchr5:152684052..152692358hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg388307
hg198307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6557725, essv6423435, essv6422167, essv5899834
SamplesHG00671, HG00589, NA18638, NA18637
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663837
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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