A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637874



Internal ID7024662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9584087..9667901hg38UCSC Ensembl
Innerchr16:9584087..9667901hg38UCSC Ensembl
Outerchr16:9583587..9668401hg38UCSC Ensembl
chr16:9677944..9761758hg19UCSC Ensembl
Innerchr16:9677944..9761758hg19UCSC Ensembl
Outerchr16:9677444..9762258hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3883815
hg1983815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15372780, essv15372781, essv15372779
SamplesNA20878, NA21129, NA21133
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637874
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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