A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4802



Internal ID15196444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186165273..186187376hg38UCSC Ensembl
Outerchr4:187086427..187108530hg19UCSC Ensembl
Outerchr4:187323421..187345524hg18UCSC Ensembl
Outerchr4:187461576..187483679hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3822104
hg1922104
hg1822104
hg1722104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4642
Supporting Variants
SamplesNA19129
Known GenesFAM149A
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)nssv4802
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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