A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8582



Internal ID15535282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:6084555..6118758hg38UCSC Ensembl
Outerchr9:6084555..6118758hg19UCSC Ensembl
Outerchr9:6074555..6108758hg18UCSC Ensembl
Outerchr9:6074555..6108758hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385236
hg195236
hg185236
hg175236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466
Supporting Variants
SamplesNA12156
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)nssv8582
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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