A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664975



Internal ID9931080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118285340..118298161hg38UCSC Ensembl
Outerchr10:118285303..118298211hg38UCSC Ensembl
Innerchr10:120044852..120057673hg19UCSC Ensembl
Outerchr10:120044815..120057723hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3812909
hg1912909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6510577
SamplesNA19679
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664975
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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