A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5569765



Internal ID9302495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88832777..89267993hg38UCSC Ensembl
Outerchr2:88832743..89268028hg38UCSC Ensembl
Innerchr2:89132290..89567750hg19UCSC Ensembl
Outerchr2:89132256..89567785hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38435286
hg19435530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676696
Supporting Variants
SamplesNA18486
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5569765
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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