A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071839



Internal ID18971713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28176935..28177336hg38UCSC Ensembl
chr18:25756899..25757300hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764721
SamplesKWP1
Known GenesCDH2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071839
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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