A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664333



Internal ID9583752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36534422..36534567hg38UCSC Ensembl
Outerchr2:36534385..36534617hg38UCSC Ensembl
Innerchr2:36761565..36761710hg19UCSC Ensembl
Outerchr2:36761528..36761760hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5846626, essv5662559, essv6125929
SamplesNA18504, NA18520, NA18505
Known GenesCRIM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664333
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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