A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5949730



Internal ID8927134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20075969..20077637hg38UCSC Ensembl
chr13:20650109..20651777hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381669
hg191669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674061
Supporting Variants
SamplesNA19372
Known GenesZMYM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5949730
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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