A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657741



Internal ID9923846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24856674..24857770hg38UCSC Ensembl
Outerchr10:24856637..24857820hg38UCSC Ensembl
Innerchr10:25145603..25146699hg19UCSC Ensembl
Outerchr10:25145566..25146749hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5581568, essv5769306
SamplesNA20588, HG00373
Known GenesPRTFDC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657741
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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