A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5609610



Internal ID8587013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59582964..59583989hg38UCSC Ensembl
chr1:60048636..60049661hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674836
Supporting Variants
SamplesNA18982
Known GenesFGGY
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5609610
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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