A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv497e214



Internal ID22756391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25814320..25825583hg38UCSC Ensembl
chr16:25825641..25836904hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3811264
hg1911264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3638283, esv3638282
SamplesHG01072
Known GenesHS3ST4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv497e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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