A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2811



Internal ID15541755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69815528..69850062hg38UCSC Ensembl
Outerchr9:72430444..72464978hg19UCSC Ensembl
Outerchr9:71620264..71654798hg18UCSC Ensembl
Outerchr9:69659998..69694532hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385493
hg195493
hg185493
hg175493
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552
Supporting Variants
SamplesNA18555
Known GenesC9orf135, C9orf135-AS1
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)nssv2811
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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