A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5439255



Internal ID8816606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14378817..14379326hg38UCSC Ensembl
Outerchr10:14378780..14379376hg38UCSC Ensembl
Innerchr10:14420816..14421325hg19UCSC Ensembl
Outerchr10:14420779..14421375hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676568
Supporting Variants
SamplesHG00259
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5439255
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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