A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9771



Internal ID15540097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:118627896..118633805hg38UCSC Ensembl
Outerchr9:121390174..121396083hg19UCSC Ensembl
Outerchr9:120429995..120435904hg18UCSC Ensembl
Outerchr9:118469728..118475637hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3813104
hg1913104
hg1813104
hg1713104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6692
Supporting Variants
SamplesNA18507
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)nssv9771
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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