A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11138



Internal ID15539441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160590042..160615932hg38UCSC Ensembl
Outerchr6:161011074..161036964hg19UCSC Ensembl
Outerchr6:160931064..160956954hg18UCSC Ensembl
Outerchr6:160981485..161007375hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3813998
hg1913998
hg1813998
hg1713998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5568
Supporting Variants
SamplesNA15510
Known GenesLPA
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)nssv11138
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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