A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385486



Internal ID5387302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15005446..15029641hg38UCSC Ensembl
chr16:15099303..15123498hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3824196
hg1924196
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638018
Supporting Variants
SamplesHG02888
Known GenesPDXDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385486
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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