A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762045



Internal ID19306928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159208791..159209592hg38UCSC Ensembl
chr5:158635799..158636600hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073509
Supporting Variants
SamplesKWP1
Known GenesRNF145
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762045
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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