A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5652925



Internal ID8945998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87516339..87516509hg38UCSC Ensembl
Outerchr10:87516302..87516559hg38UCSC Ensembl
Innerchr10:89276096..89276266hg19UCSC Ensembl
Outerchr10:89276059..89276316hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657019
Supporting Variants
SamplesHG00476
Known GenesMINPP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5652925
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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