A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667965



Internal ID9934070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8482883..8483322hg38UCSC Ensembl
chr10:8524846..8525285hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5404273, essv6506753, essv6375817, essv5767224, essv6503504, essv6302841, essv6142174, essv6044176, essv5559201, essv6287420, essv5453200
SamplesNA18486, NA20346, HG00641, HG01366, NA19138, NA19372, NA20344, NA19099, NA18501, NA19102, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667965
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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