A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7744



Internal ID15189434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36776908..36821818hg38UCSC Ensembl
Outerchr22:37172952..37217862hg19UCSC Ensembl
Outerchr22:35502898..35547808hg18UCSC Ensembl
Outerchr22:35497452..35542362hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3844911
hg1944911
hg1844911
hg1744911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3617
Supporting Variants
SamplesNA12156
Known GenesPVALB
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv7744
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer