A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4363



Internal ID15549065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:65080415..65125072hg38UCSC Ensembl
Outerchr4:65946133..65990790hg19UCSC Ensembl
Outerchr4:65628728..65673385hg18UCSC Ensembl
Outerchr4:65774899..65819556hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3844658
hg1944658
hg1844658
hg1744658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7964
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)nsv4363
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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