A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv367



Internal ID15198137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8615403..8627893hg38UCSC Ensembl
Outerchr4:8617130..8629619hg19UCSC Ensembl
Outerchr4:8668030..8680519hg18UCSC Ensembl
Outerchr4:8735201..8747690hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg389372
hg199372
hg189372
hg179372
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4225
Supporting Variants
SamplesNA19240
Known GenesCPZ
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)nssv367
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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