A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616675



Internal ID6656871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25207793..25209063hg38UCSC Ensembl
Innerchr8:25207817..25209039hg38UCSC Ensembl
Outerchr8:25207769..25209087hg38UCSC Ensembl
chr8:25065309..25066579hg19UCSC Ensembl
Innerchr8:25065333..25066555hg19UCSC Ensembl
Outerchr8:25065285..25066603hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381271
hg191271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13140653
SamplesNA20901
Known GenesDOCK5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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