A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5701724



Internal ID8679127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86196815..86197228hg38UCSC Ensembl
chr10:87956572..87956985hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666548
Supporting Variants
SamplesHG00269
Known GenesGRID1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5701724
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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