A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1856



Internal ID15546419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:70670900..70684358hg38UCSC Ensembl
Outerchr16:70704803..70718261hg19UCSC Ensembl
Outerchr16:69262304..69275762hg18UCSC Ensembl
Outerchr16:69262304..69275762hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3816448
hg1916448
hg1816448
hg1716448
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5612
SamplesNA19129
Known GenesMTSS1L
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)nsv1856
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