A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4764



Internal ID15543198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:88169158..88180963hg38UCSC Ensembl
Outerchr4:89090310..89102115hg19UCSC Ensembl
Outerchr4:89309334..89321139hg18UCSC Ensembl
Outerchr4:89447489..89459294hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg387109
hg197109
hg187109
hg177109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4415
Supporting Variants
SamplesNA19129
Known GenesABCG2
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)nssv4764
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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