A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6658



Internal ID15551589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:108156334..108187578hg38UCSC Ensembl
Outerchr9:110918614..110949858hg19UCSC Ensembl
Outerchr9:109958435..109989679hg18UCSC Ensembl
Outerchr9:107998169..108029413hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg388777
hg198777
hg188777
hg178777
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1795
SamplesNA18555
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)nsv6658
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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