A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7392



Internal ID15536472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:96822285..96866944hg38UCSC Ensembl
Outerchr1:97287841..97332500hg19UCSC Ensembl
Outerchr1:97060429..97105088hg18UCSC Ensembl
Outerchr1:96999862..97044521hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3844660
hg1944660
hg1844660
hg1744660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1966
Supporting Variants
SamplesNA12156
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)nssv7392
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