A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11034



Internal ID15539674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1570746..1619001hg38UCSC Ensembl
Outerchr20:1551392..1599647hg19UCSC Ensembl
Outerchr20:1499392..1547647hg18UCSC Ensembl
Outerchr20:1499392..1547647hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3848256
hg1948256
hg1848256
hg1748256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3253
Supporting Variants
SamplesNA15510
Known GenesSIRPB1
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)nssv11034
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