A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007089



Internal ID6719204
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3566574
SamplesHuRef
Known GenesPRC1, PRC1-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007089
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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