A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763355



Internal ID19310073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28065577..28065776hg38UCSC Ensembl
chr13:28639714..28639913hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070579
Supporting Variants
SamplesKWP1
Known GenesFLT3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763355
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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