A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1903



Internal ID15199780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:83001847..83046709hg38UCSC Ensembl
Outerchr16:83035452..83080314hg19UCSC Ensembl
Outerchr16:81592953..81637815hg18UCSC Ensembl
Outerchr16:81592953..81637815hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3844863
hg1944863
hg1844863
hg1744863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7285
SamplesNA12156
Known GenesCDH13
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)nsv1903
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