A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559



Internal ID15551480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:72273699..72295806hg38UCSC Ensembl
Outerchr9:74888615..74910722hg19UCSC Ensembl
Outerchr9:74078435..74100542hg18UCSC Ensembl
Outerchr9:72118169..72140276hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389004
hg199004
hg189004
hg179004
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6281, nssv9922
SamplesNA18507, NA12156
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)nsv6559
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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