A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675816



Internal ID9941921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89732691..89732985hg38UCSC Ensembl
chr16:89799099..89799393hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv517e199
Supporting Variantsessv6109925, essv5663155, essv5871366, essv5924197, essv6033212, essv6318464, essv5694025, essv5447889, essv5460101, essv6419170
SamplesNA11931, NA18990, NA20522, NA18952, HG01551, NA20516, NA18943, HG00620, NA20528, NA20502
Known GenesZNF276
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675816
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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