A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6588086



Internal ID9538945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78625962..78636403hg38UCSC Ensembl
Outerchr10:78625805..78636556hg38UCSC Ensembl
Innerchr10:80385719..80396160hg19UCSC Ensembl
Outerchr10:80385562..80396313hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3810752
hg1910752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658830
Supporting Variants
SamplesNA19068
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6588086
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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