A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1762



Internal ID15546325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:21198599..21227178hg38UCSC Ensembl
Outerchr16:21209920..21238499hg19UCSC Ensembl
Outerchr16:21117421..21146000hg18UCSC Ensembl
Outerchr16:21117421..21146000hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg385129
hg195129
hg185129
hg175129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2950, nssv4203
SamplesNA12878, NA18555
Known GenesZP2
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)nsv1762
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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