A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5656367



Internal ID9252421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98670820..98694106hg38UCSC Ensembl
Outerchr6:98670783..98694156hg38UCSC Ensembl
Innerchr6:99118696..99141982hg19UCSC Ensembl
Outerchr6:99118659..99142032hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3823374
hg1923374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668598
Supporting Variants
SamplesNA12144
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5656367
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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