A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4909



Internal ID15549665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:87966974..87999905hg38UCSC Ensembl
Outerchr5:87262791..87295722hg19UCSC Ensembl
Outerchr5:87298547..87331478hg18UCSC Ensembl
Outerchr5:87298547..87331478hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386772
hg196772
hg186772
hg176772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3366
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)nsv4909
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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