A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1522771



Internal ID12685893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18708170..18708220hg38UCSC Ensembl
chr20:18688814..18688864hg19UCSC Ensembl
chr20:18636814..18636864hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4364618
SamplesHuRef
Known GenesDTD1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1522771
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer