A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4789



Internal ID15543152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:151158277..151191825hg38UCSC Ensembl
Outerchr4:152079429..152112977hg19UCSC Ensembl
Outerchr4:152298879..152332427hg18UCSC Ensembl
Outerchr4:152437034..152470582hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385735
hg195735
hg185735
hg175735
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4549
Supporting Variants
SamplesNA19129
Known GenesSH3D19
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)nssv4789
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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