A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6586786



Internal ID8922116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46882536..46898449hg38UCSC Ensembl
chr1:47348208..47364121hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3815914
hg1915914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670875
Supporting Variants
SamplesHG00422
Known GenesCYP4Z2P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6586786
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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