A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637595



Internal ID6677698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:859147..890552hg38UCSC Ensembl
Innerchr16:859147..890552hg38UCSC Ensembl
Outerchr16:858647..891052hg38UCSC Ensembl
chr16:909147..940552hg19UCSC Ensembl
Innerchr16:909147..940552hg19UCSC Ensembl
Outerchr16:908647..941052hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3831406
hg1931406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355488
SamplesHG00759
Known GenesLMF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637595
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