A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7080



Internal ID15190098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:47814450..47860236hg38UCSC Ensembl
Outerchr4:47816467..47862253hg19UCSC Ensembl
Outerchr4:47511224..47557010hg18UCSC Ensembl
Outerchr4:47657395..47703181hg17UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3845787
hg1945787
hg1845787
hg1745787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4328
Supporting Variants
SamplesNA12156
Known GenesCORIN, NFXL1
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)nssv7080
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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