A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6198864



Internal ID9176267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24115187..24115497hg38UCSC Ensembl
chr16:24126508..24126818hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658327
Supporting Variants
SamplesNA18593
Known GenesPRKCB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6198864
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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