A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6331052



Internal ID9308455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152306400..152307372hg38UCSC Ensembl
chr1:152278876..152279848hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671163
Supporting Variants
SamplesNA19463
Known GenesFLG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6331052
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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