A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8046



Internal ID15189132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186171373..186215260hg38UCSC Ensembl
Outerchr4:187092527..187136414hg19UCSC Ensembl
Outerchr4:187329521..187373408hg18UCSC Ensembl
Outerchr4:187467676..187511563hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3843888
hg1943888
hg1843888
hg1743888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4642
Supporting Variants
SamplesNA12156
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)nssv8046
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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