A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6675



Internal ID15537188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:62480166..62525777hg38UCSC Ensembl
Outerchr16:62514070..62559681hg19UCSC Ensembl
Outerchr16:61071571..61117182hg18UCSC Ensembl
Outerchr16:61071571..61117182hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3845612
hg1945612
hg1845612
hg1745612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1826
Supporting Variants
SamplesNA12156
Known Genes
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)nssv6675
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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