A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4261



Internal ID15548953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:19193090..19238221hg38UCSC Ensembl
Outerchr4:19194713..19239844hg19UCSC Ensembl
Outerchr4:18803811..18848942hg18UCSC Ensembl
Outerchr4:18870982..18916113hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3845132
hg1945132
hg1845132
hg1745132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7934
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)nsv4261
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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