A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5522738



Internal ID9405235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72725459..72726167hg38UCSC Ensembl
chr13:73299597..73300305hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667348
Supporting Variants
SamplesNA18609
Known GenesMZT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5522738
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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