A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677353



Internal ID9596772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63130317..63501596hg38UCSC Ensembl
Outerchr10:63130283..63501631hg38UCSC Ensembl
Innerchr10:64890077..65261356hg19UCSC Ensembl
Outerchr10:64890043..65261391hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38371349
hg19371349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5639747
SamplesNA19130
Known GenesJMJD1C, JMJD1C-AS1, MIR1296, NRBF2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677353
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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