A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072825



Internal ID18976268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79750899..79751300hg38UCSC Ensembl
chr18:77510899..77511300hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768198
SamplesKWP1
Known GenesCTDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072825
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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