A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1234931



Internal ID12051368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33277023..33277151hg38UCSC Ensembl
chr20:31864829..31864957hg19UCSC Ensembl
chr20:31328490..31328618hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38129
hg19129
hg18129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4341173
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1234931
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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