A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5131



Internal ID15549910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:171246568..171291756hg38UCSC Ensembl
Outerchr5:170673572..170718760hg19UCSC Ensembl
Outerchr5:170606177..170651365hg18UCSC Ensembl
Outerchr5:170606177..170651365hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3845189
hg1945189
hg1845189
hg1745189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8193
SamplesNA12156
Known GenesRANBP17
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)nsv5131
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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