A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6029614



Internal ID9007017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205502041..205512020hg38UCSC Ensembl
chr1:205471169..205481148hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg389980
hg199980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657432
Supporting Variants
SamplesNA19395
Known GenesCDK18
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6029614
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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