A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616987



Internal ID6657183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41270347..41270994hg38UCSC Ensembl
Innerchr8:41270367..41270975hg38UCSC Ensembl
Outerchr8:41270328..41271014hg38UCSC Ensembl
chr8:41127866..41128513hg19UCSC Ensembl
Innerchr8:41127886..41128494hg19UCSC Ensembl
Outerchr8:41127847..41128533hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13180294
SamplesHG02793
Known GenesSFRP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616987
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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