A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1576253



Internal ID12392688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59133267..59133267hg38UCSC Ensembl
chr20:57708322..57708322hg19UCSC Ensembl
chr20:57141717..57141717hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38147
hg19147
hg18147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4288763
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1576253
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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