A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4416



Internal ID15202437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:88852738..88861235hg38UCSC Ensembl
Outerchr4:89773889..89782386hg19UCSC Ensembl
Outerchr4:89992912..90001409hg18UCSC Ensembl
Outerchr4:90131067..90139564hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg387957
hg197957
hg187957
hg177957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10412
SamplesNA18956
Known GenesFAM13A
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)nsv4416
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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