A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6449126



Internal ID9747273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62413893..62415593hg38UCSC Ensembl
chr15:62706092..62707792hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657700
Supporting Variants
SamplesNA19685
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6449126
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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