A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv422



Internal ID15544793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155951021..155970641hg38UCSC Ensembl
Outerchr4:156872173..156891793hg19UCSC Ensembl
Outerchr4:157091623..157111243hg18UCSC Ensembl
Outerchr4:157229778..157249398hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3812818
hg1912818
hg1812818
hg1712818
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4564
Supporting Variants
SamplesNA19240
Known GenesCTSO
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)nssv422
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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