A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660010



Internal ID9926115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4644861..4645462hg38UCSC Ensembl
chr10:4687053..4687654hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6448742, essv5773578, essv5871405, essv5544386, essv5965053, essv5963766, essv6212423
SamplesNA19397, NA18508, NA18507, NA18519, NA18498, NA19711, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660010
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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