A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv814



Internal ID15544685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:87895885..87915797hg38UCSC Ensembl
Outerchr9:90510800..90530712hg19UCSC Ensembl
Outerchr9:89700620..89720532hg18UCSC Ensembl
Outerchr9:87740354..87760266hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3821084
hg1921084
hg1821084
hg1721084
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6599
Supporting Variants
SamplesNA19240
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)nssv814
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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