A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666604



Internal ID9586023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15121052..15124163hg38UCSC Ensembl
chr10:15163051..15166162hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383112
hg193112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6512713
SamplesNA18538
Known GenesNMT2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666604
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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