A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6747



Internal ID15551687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133072604..133092648hg38UCSC Ensembl
Outerchr9:135947991..135968035hg19UCSC Ensembl
Outerchr9:134937812..134957856hg18UCSC Ensembl
Outerchr9:132977545..132997589hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3819463
hg1919463
hg1819463
hg1719463
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10689
SamplesNA18956
Known GenesCELP
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)nsv6747
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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