A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674575



Internal ID9940680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103086220..103099645hg38UCSC Ensembl
chr7:102726667..102740092hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3813426
hg1913426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6307653
SamplesHG01465
Known GenesARMC10, NAPEPLD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674575
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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