A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638388



Internal ID7025174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30905116..30913346hg38UCSC Ensembl
Innerchr16:30905132..30913331hg38UCSC Ensembl
Outerchr16:30905101..30913362hg38UCSC Ensembl
chr16:30916437..30924667hg19UCSC Ensembl
Innerchr16:30916453..30924652hg19UCSC Ensembl
Outerchr16:30916422..30924683hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg388231
hg198231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441765, essv15441766, essv15441767, essv15441768
SamplesNA19210, NA18879, HG03064, HG03157
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638388
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer