A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5536391



Internal ID8513794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3408736..3409178hg38UCSC Ensembl
chr1:3325300..3325742hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658512
Supporting Variants
SamplesNA18499
Known GenesPRDM16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5536391
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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