A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7045



Internal ID15190133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:161150591..161152402hg38UCSC Ensembl
Outerchr3:160868379..160870190hg19UCSC Ensembl
Outerchr3:162351073..162352884hg18UCSC Ensembl
Outerchr3:162351081..162352892hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg388753
hg198753
hg188753
hg178753
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4090
Supporting Variants
SamplesNA12156
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)nssv7045
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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