A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4806



Internal ID15549552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:39945974..39977869hg38UCSC Ensembl
Outerchr5:39946076..39977971hg19UCSC Ensembl
Outerchr5:39981833..40013728hg18UCSC Ensembl
Outerchr5:39981833..40013728hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3831896
hg1931896
hg1831896
hg1731896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9663
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)nsv4806
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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