A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637629



Internal ID7024420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2162205..2163028hg38UCSC Ensembl
Innerchr16:2162207..2163027hg38UCSC Ensembl
Outerchr16:2162204..2163030hg38UCSC Ensembl
chr16:2212206..2213029hg19UCSC Ensembl
Innerchr16:2212208..2213028hg19UCSC Ensembl
Outerchr16:2212205..2213031hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362424, essv15362418, essv15362419, essv15362422, essv15362425, essv15362421, essv15362427, essv15362420, essv15362417, essv15362426, essv15362423
SamplesHG00384, HG00318, HG00364, HG00115, HG00341, HG00346, HG00369, HG00323, NA20515, HG01200, HG00186
Known GenesTRAF7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637629
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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