A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5787987



Internal ID8765390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210367743..210374030hg38UCSC Ensembl
chr2:211232467..211238754hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg386288
hg196288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671697
Supporting Variants
SamplesHG01440
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5787987
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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