A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518



Internal ID15551435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:29350898..29381518hg38UCSC Ensembl
Outerchr9:29350896..29381516hg19UCSC Ensembl
Outerchr9:29340896..29371516hg18UCSC Ensembl
Outerchr9:29340896..29371516hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg388661
hg198661
hg188661
hg178661
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5153
SamplesNA19129
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)nsv6518
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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