A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1815



Internal ID15541098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137321588..137337501hg38UCSC Ensembl
Outerchr9:140216040..140231953hg19UCSC Ensembl
Outerchr9:139335861..139351774hg18UCSC Ensembl
Outerchr9:137491877..137507790hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg389357
hg199357
hg189357
hg179357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6770
Supporting Variants
SamplesNA18555
Known GenesEXD3
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)nssv1815
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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