A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5892938



Internal ID9003682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222200823..222207197hg38UCSC Ensembl
chr1:222374165..222380539hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg386375
hg196375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659943
Supporting Variants
SamplesHG00611
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5892938
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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