A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3309037



Internal ID15155986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116335448..116335449hg38UCSC Ensembl
Innerchr10:116335419..116335478hg38UCSC Ensembl
Outerchr10:116335418..116335479hg38UCSC Ensembl
chr10:118094960..118094961hg19UCSC Ensembl
Innerchr10:118094931..118094990hg19UCSC Ensembl
Outerchr10:118094930..118094991hg19UCSC Ensembl
chr10:118084950..118084951hg18UCSC Ensembl
Innerchr10:118084980..118084921hg18UCSC Ensembl
Outerchr10:118084920..118084981hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38219
hg19219
hg18219
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7836934
SamplesNA19239
Known GenesCCDC172
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3309037
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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