A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660299



Internal ID9926404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:124250801..124252348hg38UCSC Ensembl
Outerchr3:124250764..124252398hg38UCSC Ensembl
Innerchr3:123969648..123971195hg19UCSC Ensembl
Outerchr3:123969611..123971245hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg381635
hg191635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6375797
SamplesNA20519
Known GenesKALRN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660299
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