A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638534



Internal ID6678631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46547097..46716009hg38UCSC Ensembl
chr16:46581009..46749921hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38168913
hg19168913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15471941
SamplesHG01841
Known GenesANKRD26P1, MYLK3, ORC6, SHCBP1, VPS35
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638534
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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