A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551



Internal ID15204786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69432857..69446481hg38UCSC Ensembl
Outerchr9:72047773..72061397hg19UCSC Ensembl
Outerchr9:71237593..71251217hg18UCSC Ensembl
Outerchr9:69277327..69290951hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821689
hg1921689
hg1821689
hg1721689
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10670
SamplesNA18956
Known GenesAPBA1
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)nsv6551
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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