A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6368524



Internal ID9186745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101516158..101516790hg38UCSC Ensembl
chr10:103275915..103276547hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661408
Supporting Variants
SamplesHG01461
Known GenesBTRC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6368524
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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