A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6744



Internal ID15551684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132469839..132500519hg38UCSC Ensembl
Outerchr9:135345226..135375906hg19UCSC Ensembl
Outerchr9:134335047..134365727hg18UCSC Ensembl
Outerchr9:132374780..132405460hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg388600
hg198600
hg188600
hg178600
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5186
SamplesNA19129
Known GenesC9orf171
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)nsv6744
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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