A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15441882



Internal ID2391237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31552355..31623866hg38UCSC Ensembl
chr16:31563676..31635187hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3871512
hg1971512
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638402
Supporting Variants
SamplesHG02121
Known GenesYBX3P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15441882
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