A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1605095



Internal ID12421530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137716306..137716306hg38UCSC Ensembl
chr9:140610758..140610758hg19UCSC Ensembl
chr9:139730579..139730579hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38406
hg19406
hg18406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3629982
SamplesHuRef
Known GenesEHMT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1605095
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