A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6726



Internal ID15551664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129307474..129331602hg38UCSC Ensembl
Outerchr9:132069753..132093881hg19UCSC Ensembl
Outerchr9:131109574..131133702hg18UCSC Ensembl
Outerchr9:129149307..129173435hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386202
hg196202
hg186202
hg176202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839
SamplesNA19240
Known GenesC9orf106
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)nsv6726
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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