A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607511



Internal ID6994444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166891392..166902507hg38UCSC Ensembl
Innerchr5:166891415..166902485hg38UCSC Ensembl
Outerchr5:166891370..166902530hg38UCSC Ensembl
chr5:166318397..166329512hg19UCSC Ensembl
Innerchr5:166318420..166329490hg19UCSC Ensembl
Outerchr5:166318375..166329535hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811116
hg1911116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12124760
SamplesHG03600
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607511
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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