A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4603



Internal ID15549329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:170233956..170267521hg38UCSC Ensembl
Outerchr4:171155107..171188672hg19UCSC Ensembl
Outerchr4:171391682..171425247hg18UCSC Ensembl
Outerchr4:171529837..171563402hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg386464
hg196464
hg186464
hg176464
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3141
SamplesNA18555
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)nsv4603
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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