A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007776



Internal ID7072870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61229617..61229666hg38UCSC Ensembl
chr20:59804673..59804722hg19UCSC Ensembl
chr20:59238068..59238117hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3584526
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007776
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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