A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607159



Internal ID6994094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150333215..150348065hg38UCSC Ensembl
Innerchr5:150333222..150348058hg38UCSC Ensembl
Outerchr5:150333208..150348072hg38UCSC Ensembl
chr5:149712778..149727628hg19UCSC Ensembl
Innerchr5:149712785..149727621hg19UCSC Ensembl
Outerchr5:149712771..149727635hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3814851
hg1914851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12095956
SamplesNA19752
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607159
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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