A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638530



Internal ID6678627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46429649..46489778hg38UCSC Ensembl
chr16:46463561..46523690hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3860130
hg1960130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15471907, essv15471908, essv15471909, essv15471910
SamplesNA18964, HG00319, HG01841, HG00436
Known GenesANKRD26P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638530
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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