A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637681



Internal ID7024471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3973074..3977102hg38UCSC Ensembl
chr16:4023075..4027103hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384029
hg194029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363323
SamplesNA18618
Known GenesADCY9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637681
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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