A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6180587



Internal ID9629559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:92104469..92133887hg38UCSC Ensembl
Outerchr2:92104435..92133922hg38UCSC Ensembl
Innerchr2:92292495..92321913hg19UCSC Ensembl
Outerchr2:92292461..92321948hg19UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg3829488
hg1929488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672493
Supporting Variants
SamplesNA19352
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6180587
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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