A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4895



Internal ID15202964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:80623591..80640149hg38UCSC Ensembl
Outerchr5:79919410..79935968hg19UCSC Ensembl
Outerchr5:79955166..79971724hg18UCSC Ensembl
Outerchr5:79955166..79971724hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg388093
hg198093
hg188093
hg178093
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4848
SamplesNA19129
Known GenesDHFR
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)nsv4895
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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