A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1073866



Internal ID11890305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25077274..25077274hg38UCSC Ensembl
chr12:25230208..25230208hg19UCSC Ensembl
chr12:25121475..25121475hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38145
hg19145
hg18145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4031128
SamplesHuRef
Known GenesLRMP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1073866
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