A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3407



Internal ID15538135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:177899614..177933758hg38UCSC Ensembl
Outerchr5:177326615..177360759hg19UCSC Ensembl
Outerchr5:177259221..177293365hg18UCSC Ensembl
Outerchr5:177259221..177293365hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg385558
hg195558
hg185558
hg175558
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5151
Supporting Variants
SamplesNA12878
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)nssv3407
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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