A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617691



Internal ID7004576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75869572..75905880hg38UCSC Ensembl
chr8:76781807..76818115hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3836309
hg1936309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13234747
SamplesHG02716
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617691
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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