A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363687



Internal ID6396259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4170797..4191390hg38UCSC Ensembl
Innerchr16:4170797..4191390hg38UCSC Ensembl
Outerchr16:4170297..4191890hg38UCSC Ensembl
chr16:4220798..4241391hg19UCSC Ensembl
Innerchr16:4220798..4241391hg19UCSC Ensembl
Outerchr16:4220298..4241891hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3820594
hg1920594
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637690
Supporting Variants
SamplesNA20342
Known GenesSRL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363687
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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