A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4602



Internal ID15549328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:170140833..170180040hg38UCSC Ensembl
Outerchr4:171061984..171101191hg19UCSC Ensembl
Outerchr4:171298559..171337766hg18UCSC Ensembl
Outerchr4:171436714..171475921hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3839208
hg1939208
hg1839208
hg1739208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8028
SamplesNA12156
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)nsv4602
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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