A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732



Internal ID15549471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:15598216..15636411hg38UCSC Ensembl
Outerchr5:15598325..15636520hg19UCSC Ensembl
Outerchr5:15651325..15689520hg18UCSC Ensembl
Outerchr5:15651325..15689520hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3838196
hg1938196
hg1838196
hg1738196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8072
SamplesNA12156
Known GenesFBXL7
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)nsv4732
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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