A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15437229



Internal ID4538674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26165005..26189019hg38UCSC Ensembl
chr16:26176326..26200340hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3824015
hg1924015
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638296
Supporting Variants
SamplesHG04033
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15437229
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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