A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619155



Internal ID7006035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:145012841..145068882hg38UCSC Ensembl
chr8:146238227..146294268hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3856042
hg1956042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13372796, essv13372795
SamplesNA19092, HG03343
Known GenesC8orf33
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619155
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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