A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769411



Internal ID19308641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35761462..35763863hg38UCSC Ensembl
chr13:36335599..36338000hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075854
Supporting Variants
SamplesKWP1
Known GenesMIR548F5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769411
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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