A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638932



Internal ID6679029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69762176..69924258hg38UCSC Ensembl
chr16:69796079..69958161hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38162083
hg19162083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15503751
SamplesHG02079
Known GenesWWP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638932
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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