A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637736



Internal ID6677837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6014803..6113010hg38UCSC Ensembl
Innerchr16:6014953..6112860hg38UCSC Ensembl
Outerchr16:6014653..6113160hg38UCSC Ensembl
chr16:6064804..6163011hg19UCSC Ensembl
Innerchr16:6064954..6162861hg19UCSC Ensembl
Outerchr16:6064654..6163161hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3898208
hg1998208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv475e214
Supporting Variantsessv15364734
SamplesHG03943
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637736
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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