A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8579



Internal ID15535285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:4829645..4849963hg38UCSC Ensembl
Outerchr9:4829645..4849963hg19UCSC Ensembl
Outerchr9:4819645..4839963hg18UCSC Ensembl
Outerchr9:4819645..4839963hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385410
hg195410
hg185410
hg175410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459
Supporting Variants
SamplesNA12156
Known GenesRCL1
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)nssv8579
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