A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1324892



Internal ID12141328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36706263..36706263hg38UCSC Ensembl
chr22:37102308..37102308hg19UCSC Ensembl
chr22:35432254..35432254hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3949673
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1324892
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