A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7127



Internal ID15536737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155944539..155958237hg38UCSC Ensembl
Outerchr4:156865691..156879389hg19UCSC Ensembl
Outerchr4:157085141..157098839hg18UCSC Ensembl
Outerchr4:157223296..157236994hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3811794
hg1911794
hg1811794
hg1711794
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4564
Supporting Variants
SamplesNA12156
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)nssv7127
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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