A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020628



Internal ID22082259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9268546..9286961hg38UCSC Ensembl
Outerchr5:9264570..9291176hg38UCSC Ensembl
Innerchr5:9268658..9287073hg19UCSC Ensembl
Outerchr5:9264682..9291288hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3826607
hg1926607
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156309
Supporting Variants
Samples
Known GenesSEMA5A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020628
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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