A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1679513



Internal ID12842631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62875229..62875510hg38UCSC Ensembl
chr20:61506581..61506862hg19UCSC Ensembl
chr20:60977026..60977307hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38282
hg19282
hg18282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3840238
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1679513
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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