A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073861



Internal ID19323412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13399845..13399920hg38UCSC Ensembl
chr5:13399957..13400032hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764799
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073861
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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