A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389



Internal ID15202407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:73824830..73856555hg38UCSC Ensembl
Outerchr4:74690547..74722272hg19UCSC Ensembl
Outerchr4:74909411..74941136hg18UCSC Ensembl
Outerchr4:75055582..75087307hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg388296
hg198296
hg188296
hg178296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2470
SamplesNA18555
Known GenesCXCL6, PF4V1
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)nsv4389
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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