A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6300445



Internal ID8974680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89062379..89071310hg38UCSC Ensembl
Outerchr10:89062345..89071345hg38UCSC Ensembl
Innerchr10:90822136..90831067hg19UCSC Ensembl
Outerchr10:90822102..90831102hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667444
Supporting Variants
SamplesHG00554
Known GenesMIR4679-1, MIR4679-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6300445
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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