A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1879



Internal ID15546442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75310682..75345394hg38UCSC Ensembl
Outerchr16:75344580..75379292hg19UCSC Ensembl
Outerchr16:73902081..73936793hg18UCSC Ensembl
Outerchr16:73902081..73936793hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg385036
hg195036
hg185036
hg175036
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4228
SamplesNA12878
Known GenesCFDP1
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)nsv1879
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