A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677708



Internal ID9943813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44598919..44601292hg38UCSC Ensembl
chr10:45094367..45096740hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382374
hg192374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5626933, essv5416878, essv5959222
SamplesHG00330, HG00311, HG00278
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677708
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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