A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660852



Internal ID9580271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97983249..97983586hg38UCSC Ensembl
chr10:99743006..99743343hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6180993, essv5448085, essv5989922, essv5819320, essv5940247, essv6509643, essv6346740, essv6244196, essv6276489, essv5929432
SamplesNA18861, NA19819, NA19397, NA19129, NA19393, NA18510, NA19138, NA18907, NA18909, NA19394
Known GenesCRTAC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660852
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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