A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15492884



Internal ID6716824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59945099..59955205hg38UCSC Ensembl
chr16:59979003..59989109hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3810107
hg1910107
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638754
Supporting Variants
SamplesNA20849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15492884
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