A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637647



Internal ID6677750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3055679..3070944hg38UCSC Ensembl
chr16:3105680..3120945hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3815266
hg1915266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362844, essv15362845, essv15362846
SamplesNA20585, NA19141, HG02923
Known GenesIL32, MMP25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637647
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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