A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3840238



Internal ID11921633
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1679513
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3840238
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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