A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638020



Internal ID6678118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15031082..15082591hg38UCSC Ensembl
chr16:15124939..15176448hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3851510
hg1951510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385523, essv15385524
SamplesHG00766, HG01464
Known GenesNTAN1, PDXDC1, RRN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638020
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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