A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4133



Internal ID15202126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:177831191..177865858hg38UCSC Ensembl
Outerchr3:177548979..177583646hg19UCSC Ensembl
Outerchr3:179031673..179066340hg18UCSC Ensembl
Outerchr3:179031681..179066348hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385362
hg195362
hg185362
hg175362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3118
SamplesNA18555
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)nsv4133
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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