A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670749



Internal ID9590168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36256595..36266438hg38UCSC Ensembl
Outerchr20:36256558..36266488hg38UCSC Ensembl
Innerchr20:34844517..34854360hg19UCSC Ensembl
Outerchr20:34844480..34854410hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389931
hg199931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5577836
SamplesNA19676
Known GenesAAR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670749
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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