A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5170



Internal ID15542872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:96098705..96132573hg38UCSC Ensembl
Outerchr9:98860987..98894855hg19UCSC Ensembl
Outerchr9:97900808..97934676hg18UCSC Ensembl
Outerchr9:95940542..95974410hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385413
hg195413
hg185413
hg175413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6622
Supporting Variants
SamplesNA19129
Known GenesLOC158434, LOC158435
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)nssv5170
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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