A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768999



Internal ID18964315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17777295..17777366hg38UCSC Ensembl
chr19:17888104..17888175hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071918
Supporting Variants
SamplesKWP1
Known GenesFCHO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768999
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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