A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6158627



Internal ID9805079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3914050..3915513hg38UCSC Ensembl
Outerchr20:3914013..3915563hg38UCSC Ensembl
Innerchr20:3894697..3896160hg19UCSC Ensembl
Outerchr20:3894660..3896210hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381551
hg191551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668086
Supporting Variants
SamplesNA19904
Known GenesPANK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6158627
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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