A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11243



Internal ID15539336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122575775..122587364hg38UCSC Ensembl
Outerchr10:124335291..124346880hg19UCSC Ensembl
Outerchr10:124325281..124336870hg18UCSC Ensembl
Outerchr10:124325281..124336870hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3812857
hg1912857
hg1812857
hg1712857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7582
Supporting Variants
SamplesNA15510
Known GenesDMBT1
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)nssv11243
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