A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6078084



Internal ID9684035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125191916..125193376hg38UCSC Ensembl
Outerchr10:125191864..125193442hg38UCSC Ensembl
Innerchr10:126880485..126881945hg19UCSC Ensembl
Outerchr10:126880433..126882011hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381579
hg191579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663002
Supporting Variants
SamplesNA19435
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6078084
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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