A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4455



Internal ID15549166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:107174142..107231013hg38UCSC Ensembl
Outerchr4:108095299..108152170hg19UCSC Ensembl
Outerchr4:108314748..108371619hg18UCSC Ensembl
Outerchr4:108452903..108509774hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3856872
hg1956872
hg1856872
hg1756872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3274, nssv7112
SamplesNA12156, NA12878
Known Genes
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)nsv4455
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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