A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1782



Internal ID15194379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:34984490..35015049hg38UCSC Ensembl
Outerchr9:34984487..35015046hg19UCSC Ensembl
Outerchr9:34974487..35005046hg18UCSC Ensembl
Outerchr9:34974487..35005046hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg389472
hg199472
hg189472
hg179472
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527
Supporting Variants
SamplesNA18555
Known GenesDNAJB5, LOC101926900
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)nssv1782
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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