A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616424



Internal ID7003311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16023868..16498645hg38UCSC Ensembl
Innerchr8:16024018..16498495hg38UCSC Ensembl
Outerchr8:16023718..16498795hg38UCSC Ensembl
chr8:15881377..16356154hg19UCSC Ensembl
Innerchr8:15881527..16356004hg19UCSC Ensembl
Outerchr8:15881227..16356304hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38474778
hg19474778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13118968
SamplesHG03788
Known GenesMSR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616424
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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