A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072808



Internal ID18971819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62715166..62716067hg38UCSC Ensembl
chr18:60382399..60383300hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764058
SamplesKWP1
Known GenesPHLPP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072808
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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