A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6569411



Internal ID9546814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168754628..168755993hg38UCSC Ensembl
chr4:169675779..169677144hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673045
Supporting Variants
SamplesNA18574
Known GenesPALLD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6569411
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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