A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4353



Internal ID15549054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:59826015..59844918hg38UCSC Ensembl
Outerchr4:60691733..60710636hg19UCSC Ensembl
Outerchr4:60374328..60393231hg18UCSC Ensembl
Outerchr4:60520499..60539402hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3817772
hg1917772
hg1817772
hg1717772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9643
SamplesNA18507
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)nsv4353
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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