A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657288



Internal ID9923393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31752107..31759261hg38UCSC Ensembl
chr10:32041035..32048189hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387155
hg197155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127e199
Supporting Variantsessv5813973, essv5658715, essv5599109
SamplesHG01070, NA18523, NA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657288
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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