A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13118989



Internal ID3120805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16089605..16164358hg38UCSC Ensembl
chr8:15947114..16021867hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3874754
hg1974754
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616431
Supporting Variants
SamplesHG03746
Known GenesMSR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13118989
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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