A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4457



Internal ID15202482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:107910943..107941846hg38UCSC Ensembl
Outerchr4:108832099..108863002hg19UCSC Ensembl
Outerchr4:109051548..109082451hg18UCSC Ensembl
Outerchr4:109189703..109220606hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg388376
hg198376
hg188376
hg178376
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4775
SamplesNA19129
Known GenesCYP2U1, SGMS2
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)nsv4457
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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