A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363268



Internal ID5365084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3702100..3704001hg38UCSC Ensembl
Innerchr16:3702102..3704000hg38UCSC Ensembl
Outerchr16:3702099..3704003hg38UCSC Ensembl
chr16:3752101..3754002hg19UCSC Ensembl
Innerchr16:3752103..3754001hg19UCSC Ensembl
Outerchr16:3752100..3754004hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637674
Supporting Variants
SamplesHG02455
Known GenesTRAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363268
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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