A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4906



Internal ID15549662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:84394208..84426970hg38UCSC Ensembl
Outerchr5:83690026..83722788hg19UCSC Ensembl
Outerchr5:83725782..83758544hg18UCSC Ensembl
Outerchr5:83725782..83758544hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386672
hg196672
hg186672
hg176672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6009
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)nsv4906
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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