A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5833085



Internal ID9310562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101631154..101633218hg38UCSC Ensembl
Outerchr1:101631117..101633268hg38UCSC Ensembl
Innerchr1:102096710..102098774hg19UCSC Ensembl
Outerchr1:102096673..102098824hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659633
Supporting Variants
SamplesNA18501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5833085
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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