A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4269



Internal ID15548961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:21759806..21804433hg38UCSC Ensembl
Outerchr4:21761429..21806056hg19UCSC Ensembl
Outerchr4:21370527..21415154hg18UCSC Ensembl
Outerchr4:21437698..21482325hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3844628
hg1944628
hg1844628
hg1744628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7936
SamplesNA12156
Known GenesKCNIP4
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)nsv4269
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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