A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5980958



Internal ID9579110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1580345..1613395hg38UCSC Ensembl
chr20:1560991..1594041hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833051
hg1933051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673583
Supporting Variants
SamplesNA19152
Known GenesSIRPB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5980958
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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