A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5165



Internal ID15542891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:83260524..83294417hg38UCSC Ensembl
Outerchr9:85875439..85909332hg19UCSC Ensembl
Outerchr9:85065259..85099152hg18UCSC Ensembl
Outerchr9:83104993..83138886hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg385392
hg195392
hg185392
hg175392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588
Supporting Variants
SamplesNA19129
Known GenesFRMD3
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)nssv5165
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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