A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446



Internal ID15203570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111885800..111915135hg38UCSC Ensembl
Outerchr6:112207003..112236338hg19UCSC Ensembl
Outerchr6:112313696..112343031hg18UCSC Ensembl
Outerchr6:112313696..112343031hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3829336
hg1929336
hg1829336
hg1729336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9894, nssv577
SamplesNA18507, NA19240
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)nsv5446
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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