A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363717



Internal ID6326579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4652859..4677716hg38UCSC Ensembl
chr16:4702860..4727717hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3824858
hg1924858
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637699
Supporting Variants
SamplesNA19921
Known GenesMGRN1, MIR6769A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363717
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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