A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662551



Internal ID9928656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128209288..128209339hg38UCSC Ensembl
chr10:130007552..130007603hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5607839, essv6331733, essv6478991, essv6578145, essv6071759, essv6040697, essv5445804, essv5996637, essv5752880, essv6027791, essv6004061, essv5932838, essv6218874, essv6412653
SamplesNA07357, NA18519, NA12891, NA18942, NA12044, NA19239, NA18973, NA12878, NA12892, NA19099, NA12144, NA18858, NA18909, NA19240
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662551
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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