A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616946



Internal ID7003832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39306341..39311245hg38UCSC Ensembl
Innerchr8:39306341..39311245hg38UCSC Ensembl
Outerchr8:39306131..39311445hg38UCSC Ensembl
chr8:39163860..39168764hg19UCSC Ensembl
Innerchr8:39163860..39168764hg19UCSC Ensembl
Outerchr8:39163650..39168964hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg384905
hg194905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13170750, essv13170751
SamplesHG00409, NA18577
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616946
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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