A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579



Internal ID15551502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:79951344..79985030hg38UCSC Ensembl
Outerchr9:82566259..82599945hg19UCSC Ensembl
Outerchr9:81756079..81789765hg18UCSC Ensembl
Outerchr9:79795813..79829499hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385558
hg195558
hg185558
hg175558
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5163
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)nsv6579
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