A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1842



Internal ID15199719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:67705002..67725686hg38UCSC Ensembl
Outerchr16:67738905..67759589hg19UCSC Ensembl
Outerchr16:66296406..66317090hg18UCSC Ensembl
Outerchr16:66296406..66317090hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg388627
hg198627
hg188627
hg178627
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6677, nssv5609, nssv1313
SamplesNA19129, NA12156, NA19240
Known GenesGFOD2, RANBP10
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)nsv1842
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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