A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616944



Internal ID7003830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39283573..39299988hg38UCSC Ensembl
Innerchr8:39283584..39299977hg38UCSC Ensembl
Outerchr8:39283562..39299999hg38UCSC Ensembl
chr8:39141092..39157507hg19UCSC Ensembl
Innerchr8:39141103..39157496hg19UCSC Ensembl
Outerchr8:39141081..39157518hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3816416
hg1916416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13170747, essv13170746, essv13170748
SamplesHG00356, HG00266, HG00273
Known GenesADAM32
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616944
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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