A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618134



Internal ID7005017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97174500..97208268hg38UCSC Ensembl
chr8:98186728..98220496hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833769
hg1933769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13266950
SamplesHG03943
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618134
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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