A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15354661



Internal ID5356477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65681..100253hg38UCSC Ensembl
chr16:115679..150251hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3834573
hg1934573
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637537
Supporting Variants
SamplesHG00524
Known GenesMPG, NPRL3, RHBDF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15354661
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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