A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4160



Internal ID15548842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:188050512..188060859hg38UCSC Ensembl
Outerchr3:187768300..187778647hg19UCSC Ensembl
Outerchr3:189250994..189261341hg18UCSC Ensembl
Outerchr3:189251002..189261349hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg386296
hg196296
hg186296
hg176296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3121
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)nsv4160
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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