A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482



Internal ID15204710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:14673697..14718570hg38UCSC Ensembl
Outerchr9:14673695..14718568hg19UCSC Ensembl
Outerchr9:14663695..14708568hg18UCSC Ensembl
Outerchr9:14663695..14708568hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3844874
hg1944874
hg1844874
hg1744874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5149
SamplesNA19129
Known GenesZDHHC21
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)nsv6482
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