A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6355299



Internal ID9016231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32305232..32306946hg38UCSC Ensembl
chr20:30893035..30894749hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381715
hg191715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670812
Supporting Variants
SamplesHG00629
Known GenesKIF3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6355299
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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