A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618214



Internal ID7005097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101987327..102007840hg38UCSC Ensembl
chr8:102999555..103020068hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3820514
hg1920514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13269720
SamplesHG02854
Known GenesNCALD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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