A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763356



Internal ID19315248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35864258..35864587hg38UCSC Ensembl
chr13:36438395..36438724hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070582
Supporting Variants
SamplesKWP1
Known GenesDCLK1, MIR548F5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763356
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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