A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10010882



Internal ID5690480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89201593..89211606hg38UCSC Ensembl
chr1:89667276..89677289hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810014
hg1910014
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3586755
Supporting Variants
SamplesNA19085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10010882
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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