A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8063



Internal ID15535801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:9879032..9923808hg38UCSC Ensembl
Outerchr5:9879144..9923920hg19UCSC Ensembl
Outerchr5:9932144..9976920hg18UCSC Ensembl
Outerchr5:9932144..9976920hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844777
hg1944777
hg1844777
hg1744777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4712
Supporting Variants
SamplesNA12156
Known GenesLOC285692
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)nssv8063
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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