A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677148



Internal ID9943253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65805555..65811314hg38UCSC Ensembl
chr15:66097893..66103652hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385760
hg195760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5680219, essv6110989, essv5741365, essv5465086, essv6506038, essv6308351, essv5683845
SamplesHG00640, HG01069, NA19235, HG01048, NA18908, HG00731, HG01190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677148
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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