A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4642



Internal ID15202686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186164028..186215260hg38UCSC Ensembl
Outerchr4:187085182..187136414hg19UCSC Ensembl
Outerchr4:187322176..187373408hg18UCSC Ensembl
Outerchr4:187460331..187511563hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3851233
hg1951233
hg1851233
hg1751233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2497, nssv3310, nssv4802, nssv8046
SamplesNA12156, NA12878, NA18555, NA19129
Known GenesCYP4V2, FAM149A, FLJ38576
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)nsv4642
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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