A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5098



Internal ID15549873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:160749621..160771155hg38UCSC Ensembl
Outerchr5:160176628..160198162hg19UCSC Ensembl
Outerchr5:160109206..160130740hg18UCSC Ensembl
Outerchr5:160109206..160130740hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3816044
hg1916044
hg1816044
hg1716044
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9416
SamplesNA18517
Known GenesATP10B
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)nsv5098
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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