A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3722656



Internal ID12039214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83158750..83158750hg38UCSC Ensembl
chr9:85773665..85773665hg19UCSC Ensembl
chr9:84963485..84963485hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1550653
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3722656
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