A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6629



Internal ID15551557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98449035..98482700hg38UCSC Ensembl
Outerchr9:101211317..101244982hg19UCSC Ensembl
Outerchr9:100251138..100284803hg18UCSC Ensembl
Outerchr9:98290872..98324537hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385774
hg195774
hg185774
hg175774
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8640
SamplesNA12156
Known GenesGABBR2
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)nsv6629
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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