A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6286



Internal ID15537577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:87917239..87921269hg38UCSC Ensembl
Outerchr9:90532154..90536184hg19UCSC Ensembl
Outerchr9:89721974..89726004hg18UCSC Ensembl
Outerchr9:87761708..87765738hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3816473
hg1916473
hg1816473
hg1716473
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6599
Supporting Variants
SamplesNA12156
Known GenesSPATA31C1
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)nssv6286
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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