A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11022



Internal ID15539686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:146103282..146128234hg38UCSC Ensembl
Outerchr2:146860850..146885802hg19UCSC Ensembl
Outerchr2:146577320..146602272hg18UCSC Ensembl
Outerchr2:146694582..146719534hg17UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3824953
hg1924953
hg1824953
hg1724953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2960
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11022
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