A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5643606



Internal ID9751063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61055011..61058422hg38UCSC Ensembl
Outerchr2:61054854..61058588hg38UCSC Ensembl
Innerchr2:61282146..61285557hg19UCSC Ensembl
Outerchr2:61281989..61285723hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg383735
hg193735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674794
Supporting Variants
SamplesNA19701
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5643606
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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