A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9835



Internal ID15539902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:33223366..33256764hg38UCSC Ensembl
Outerchr12:33376301..33409699hg19UCSC Ensembl
Outerchr12:33267568..33300966hg18UCSC Ensembl
Outerchr12:33267568..33300966hg17UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3833399
hg1933399
hg1833399
hg1733399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv669
Supporting Variants
SamplesNA18507
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)nssv9835
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