A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606836



Internal ID6993771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133887183..133888538hg38UCSC Ensembl
Innerchr5:133887191..133888530hg38UCSC Ensembl
Outerchr5:133887175..133888546hg38UCSC Ensembl
chr5:133222874..133224229hg19UCSC Ensembl
Innerchr5:133222882..133224221hg19UCSC Ensembl
Outerchr5:133222866..133224237hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381356
hg191356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12066398
SamplesNA19119
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606836
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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