A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6370889



Internal ID9348292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168055321..168056494hg38UCSC Ensembl
chr1:168024559..168025732hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672177
Supporting Variants
SamplesNA19725
Known GenesDCAF6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6370889
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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