A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663266



Internal ID9929371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30936518..30940531hg38UCSC Ensembl
chr13:31510655..31514668hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg384014
hg194014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5492004, essv6442159
SamplesNA19359, NA19390
Known GenesTEX26
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663266
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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