A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3606362



Internal ID6993298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115297718..115298741hg38UCSC Ensembl
Innerchr5:115297718..115298741hg38UCSC Ensembl
Outerchr5:115297507..115298949hg38UCSC Ensembl
chr5:114633415..114634438hg19UCSC Ensembl
Innerchr5:114633415..114634438hg19UCSC Ensembl
Outerchr5:114633204..114634646hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg381024
hg191024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12026246
SamplesHG00154
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3606362
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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