A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4560



Internal ID15549282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:154672973..154717481hg38UCSC Ensembl
Outerchr4:155594125..155638633hg19UCSC Ensembl
Outerchr4:155813575..155858083hg18UCSC Ensembl
Outerchr4:155951730..155996238hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3844509
hg1944509
hg1844509
hg1744509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8016
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)nsv4560
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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