A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4395



Internal ID15549100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:77608286..77643412hg38UCSC Ensembl
Outerchr4:78529440..78564566hg19UCSC Ensembl
Outerchr4:78748464..78783590hg18UCSC Ensembl
Outerchr4:78886619..78921745hg17UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg384622
hg194622
hg184622
hg174622
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3264
SamplesNA12878
Known GenesCXCL13
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)nsv4395
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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