A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670096



Internal ID9936201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37335159..37339553hg38UCSC Ensembl
chr21:38707461..38711855hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg384395
hg194395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5551575, essv6278282, essv6376681
SamplesNA19446, NA19449, NA19435
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670096
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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