A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5978756



Internal ID8956159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35039357..35041511hg38UCSC Ensembl
Outerchr1:35039200..35041664hg38UCSC Ensembl
Innerchr1:35504958..35507112hg19UCSC Ensembl
Outerchr1:35504801..35507265hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382465
hg192465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661048
Supporting Variants
SamplesHG00560
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5978756
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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