A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670111



Internal ID9589530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92319545..92322987hg38UCSC Ensembl
chr10:94079302..94082744hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383443
hg193443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5677056, essv6475863, essv6181270, essv6291932, essv6149172, essv5475430, essv6462351
SamplesNA19350, NA19374, NA19384, NA20342, NA19451, NA19467, NA19431
Known GenesMARCH5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670111
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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