A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5620706



Internal ID9634387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27653140..27653997hg38UCSC Ensembl
chr1:27979651..27980508hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677722
Supporting Variants
SamplesNA19360
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5620706
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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