A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6727



Internal ID15551665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129354025..129356337hg38UCSC Ensembl
Outerchr9:132116304..132118616hg19UCSC Ensembl
Outerchr9:131156125..131158437hg18UCSC Ensembl
Outerchr9:129195858..129198170hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3815388
hg1915388
hg1815388
hg1715388
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10686
SamplesNA18956
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)nsv6727
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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