A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372183



Internal ID1749566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8877335..8935781hg38UCSC Ensembl
chr16:8971192..9029638hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3858447
hg1958447
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637852
Supporting Variants
SamplesHG01615
Known GenesUSP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372183
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