A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3823298



Internal ID11591887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156328046..156328046hg38UCSC Ensembl
chr1:156297837..156297837hg19UCSC Ensembl
chr1:154564461..154564461hg18UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38142
hg19142
hg18142
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1449360
Supporting Variants
SamplesHuRef
Known GenesCCT3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3823298
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