A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657861



Internal ID9577280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3627957..3630656hg38UCSC Ensembl
Outerchr11:3627923..3630691hg38UCSC Ensembl
Innerchr11:3649187..3651886hg19UCSC Ensembl
Outerchr11:3649153..3651921hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382769
hg192769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv186e199
Supporting Variantsessv6306147, essv5810472
SamplesHG00671, HG00620
Known GenesTRPC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657861
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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