A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4226



Internal ID15202228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8614800..8654556hg38UCSC Ensembl
Outerchr4:8616527..8656282hg19UCSC Ensembl
Outerchr4:8667427..8707182hg18UCSC Ensembl
Outerchr4:8734598..8774353hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3839757
hg1939756
hg1839756
hg1739756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9878, nssv4725
SamplesNA18507, NA19129
Known GenesCPZ
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)nsv4226
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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