A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663520



Internal ID9929625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:98332714..98348945hg38UCSC Ensembl
Outerchr1:98332677..98348995hg38UCSC Ensembl
Innerchr1:98798270..98814501hg19UCSC Ensembl
Outerchr1:98798233..98814551hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3816319
hg1916319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6569600
SamplesHG00436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663520
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