A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616915



Internal ID7003801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38062893..38091759hg38UCSC Ensembl
Innerchr8:38062895..38091757hg38UCSC Ensembl
Outerchr8:38062891..38091761hg38UCSC Ensembl
chr8:37920411..37949277hg19UCSC Ensembl
Innerchr8:37920413..37949275hg19UCSC Ensembl
Outerchr8:37920409..37949279hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3828867
hg1928867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13169019, essv13169018, essv13169017, essv13169020, essv13169016
SamplesHG02784, HG03705, HG03663, HG03021, HG02725
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616915
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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