A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6025169



Internal ID9002572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110749813..110750366hg38UCSC Ensembl
chr6:111071016..111071569hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672817
Supporting Variants
SamplesNA19921
Known GenesCDK19
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6025169
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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