A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6290612



Internal ID9396346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25994417..25998516hg38UCSC Ensembl
Outerchr2:25994380..25998566hg38UCSC Ensembl
Innerchr2:26217286..26221385hg19UCSC Ensembl
Outerchr2:26217249..26221435hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658052
Supporting Variants
SamplesNA18599
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6290612
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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