A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663139



Internal ID9582558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102837260..102838700hg38UCSC Ensembl
chr11:102707991..102709431hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381441
hg191441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6227339, essv6523243
SamplesHG00330, HG00324
Known GenesMMP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663139
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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