A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv791



Internal ID15544623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:6352439..6356712hg38UCSC Ensembl
Outerchr9:6352439..6356712hg19UCSC Ensembl
Outerchr9:6342439..6346712hg18UCSC Ensembl
Outerchr9:6342439..6346712hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385853
hg195853
hg185853
hg175853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467
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)nssv791
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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