A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763135



Internal ID18962175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18542889..18543890hg38UCSC Ensembl
chr19:18653699..18654700hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071921
Supporting Variants
SamplesKWP1
Known GenesFKBP8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763135
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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