A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1174496



Internal ID11990933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112525991..112525991hg38UCSC Ensembl
chr9:115288271..115288271hg19UCSC Ensembl
chr9:114328092..114328092hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38138
hg19138
hg18138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3985655
SamplesHuRef
Known GenesKIAA1958
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1174496
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