A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071874



Internal ID18977256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78978999..78980600hg38UCSC Ensembl
chr18:76738999..76740600hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768819
SamplesKWP1
Known GenesSALL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071874
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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