A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4331



Internal ID15549030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49263264..49320480hg38UCSC Ensembl
Outerchr4:49265281..49322497hg19UCSC Ensembl
Outerchr4:48960038..49017254hg18UCSC Ensembl
Outerchr4:49106209..49163425hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3857217
hg1957217
hg1857217
hg1757217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3253
SamplesNA12878
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)nsv4331
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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