A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1307442



Internal ID12123879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90974460..90974460hg38UCSC Ensembl
chr15:91517690..91517690hg19UCSC Ensembl
chr15:89318694..89318694hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4257033
SamplesHuRef
Known GenesPRC1, PRC1-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1307442
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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