A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666228



Internal ID9585647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1423568..1423768hg38UCSC Ensembl
chr10:1465763..1465963hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5852175, essv6350983, essv6153949, essv6092436, essv6125955, essv6465751, essv6371983, essv5582106
SamplesHG00323, HG01173, HG00337, NA20754, HG00185, HG00282, HG01080, NA11830
Known GenesADARB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666228
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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