A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620808



Internal ID7007678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78819110..78879140hg38UCSC Ensembl
chr9:81434026..81494056hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3860031
hg1960031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13533015, essv13533016, essv13533017
SamplesNA18907, NA19116, NA18505
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620808
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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