A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3362



Internal ID15538090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:77813181..77815465hg38UCSC Ensembl
Outerchr5:77109005..77111289hg19UCSC Ensembl
Outerchr5:77144761..77147045hg18UCSC Ensembl
Outerchr5:77144761..77147045hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg386192
hg196192
hg186192
hg176192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4890
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)nssv3362
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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