A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664182



Internal ID9930287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128679512..128683918hg38UCSC Ensembl
Outerchr10:128679355..128684071hg38UCSC Ensembl
Innerchr10:130477776..130482182hg19UCSC Ensembl
Outerchr10:130477619..130482335hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg384717
hg194717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5581186
SamplesHG00626
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664182
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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