A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3566574



Internal ID6691270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90974368..90974368hg38UCSC Ensembl
chr15:91517598..91517598hg19UCSC Ensembl
chr15:89318602..89318602hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007089
Supporting Variants
SamplesHuRef
Known GenesPRC1, PRC1-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3566574
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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