A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6035



Internal ID15537829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:159419825..159452295hg38UCSC Ensembl
Outerchr5:158846833..158879303hg19UCSC Ensembl
Outerchr5:158779411..158811881hg18UCSC Ensembl
Outerchr5:158779411..158811881hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg386965
hg196965
hg186965
hg176965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5095
Supporting Variants
SamplesNA12156
Known GenesLOC285627
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)nssv6035
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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