A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662740



Internal ID9582159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32233384..32235370hg38UCSC Ensembl
Outerchr1:32233347..32235420hg38UCSC Ensembl
Innerchr1:32698985..32700971hg19UCSC Ensembl
Outerchr1:32698948..32701021hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382074
hg192074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6509961
SamplesHG00246
Known GenesMTMR9LP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662740
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