A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672666



Internal ID9592085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:16751392..16753743hg38UCSC Ensembl
Outerchr2:16751358..16753778hg38UCSC Ensembl
Innerchr2:16932659..16935010hg19UCSC Ensembl
Outerchr2:16932625..16935045hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv684e199
Supporting Variantsessv6418154
SamplesNA19703
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672666
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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